A hydrogen permeation membrane is provided that can include a carbon-based material (C) and a ceramic material (BZCYT) mixed together. The carbon-based material can include graphene, graphite, carbon nanotubes, or a combination thereof. The ceramic material can have the formula BaZr.sub.1-x-y-zCe.sub.xY.sub.yT.sub.zO.sub.3-?, where 0?x?0.5, 0?y?0.5, 0?z?0.5, (x+y+z)>0; 0???0.5, and T is Yb, Sc, Ti, Nb, Ta, Mo, Mn, Fe, Co, Ni, Cu, Zn, Ga, In, or a combination thereof. In addition, the BZYCT can be present in the C-BZCYT mixture in an amount ranging from about 40% by volume to about 80% by volume. Further, a method of forming such a membrane is also provided. A method is also provided for extracting hydrogen from a feed stream.

An apparatus for fabricating a graphene membrane includes a first section having a first fluid chamber for housing a suspension of graphene platelets in a fluid. A second section is positionable adjacent the first section. The second section has a second fluid chamber and a porous support housed in the second fluid chamber for supporting a porous substrate. When the first section is positioned adjacent to the second section and the porous substrate is supported by the porous support, the first fluid chamber and the second fluid chamber are in fluid communication via the porous substrate. The apparatus further includes a pressurizer for creating a pressure differential between the first fluid chamber and the second fluid chamber and thereby forcing the fluid through the porous substrate and into the second fluid chamber and lodging the graphene platelets in the pores of the porous substrate.

New carbon nanomaterials, preferably titanium carbide-derived carbon (CDC) nanoparticles, were embedded into a polyamide film to give CDC/polyamide mixed matrix membranes by the interfacial polymerization reaction of an aliphatic diamine, e.g., piperazine, and an activated aromatic dicarboxylate, e.g., isophthaloyl chloride, supported on a sulfone-containing polymer, e.g., polysulfone (PSF), layer, which is preferably previously prepared by dry/wet phase inversion. The inventive membranes can separate CO.sub.2 (or other gases) from mixtures of CO.sub.2 and further gases, esp. CH.sub.4, based upon the generally selective nanocomposite layer(s) of CDC/polyamide.

The present disclosure relates to sustainable and green polylactic acid-based membranes embedded with self-assembled positively and negatively charged multiwalled carbon nanotube/graphene oxide nanohybrids for the removal of organic and inorganic nutrients from wastewater, and methods of synthesis of the same. A positively charged multi-walled carbon nanotube/graphene oxide (f-MWCNT/GO) nanohybrid-based mixed matrix membrane can comprise a self-assembled multi-walled carbon nanotube and graphene oxide (f-MWCNT/GO) nanohybrid, and a polylactic acid (PLA) membrane matrix. The f-MWCNT/GO nanohybrid is integrated into the PLA membrane matrix to form the positively charged mixed matrix membrane. A negatively charged multi-walled carbon nanotubes (f-GO/MWCNTs-COOH) nanohybrid-based mixed matrix membrane can comprise a positively charged Graphene Oxide and negatively charged multi-walled carbon nanotube-COOH (f-GO/MWCNTs-COOH) nanohybrid, and a polylactic acid (PLA) membrane matrix. The f-GO/MWCNTs-COOH nanohybrid is integrated into the PLA membrane matrix to form the negatively charged mixed matrix membrane.

The embodiments of the present disclosure relate to a method and apparatus for producing a carbon nanomaterial product (CNM) product that may comprise carbon nanotubes and various other allotropes of nanocarbon. The method and apparatus employ a consumable carbon dioxide (CO.sub.2) and a renewable carbonate electrolyte as reactants in an electrolysis reaction in order to make CNTs. In some embodiments of the present disclosure, operational conditions of the electrolysis reaction may be varied in order to produce the CNM product with a greater incidence of a desired allotrope of nanocarbon or a desired combination of two or more allotropes.

Composite nanostructures having a crumpled graphene oxide shell and a nanoparticle selected from titanium dioxide, silver and magnetite within the shell are disclosed. The nanostructures may be incorporated into a filtration membrane suitable for purifying water for targeted separations and for human consumption.

Membranes of the present disclosure possess very thin barrier layers, with high selectivity, high throughput, low fouling, and are long lasting. The membranes include graphene and/or graphene oxide barrier layers on a nanofibrous supporting scaffold. Methods for forming these membranes, as well as uses thereof, are also provided. In embodiments, an article of the present disclosure includes a nanofibrous scaffold; at least a first layer of nanoporous graphene, nanoporous graphene oxide, or combinations thereof on at least a portion of a surface of the nanofibrous scaffold; an additive such as crosslinking agents and/or particles on an outer surface of the at least first layer of nanoporous graphene, nanoporous graphene oxide, or combinations thereof.

The invention, belonging to the field of membrane technology, presents a method for the high-throughput preparation of carbon nanotube hollow fiber membranes. This method contains three major steps. Firstly, the pristine carbon nanotubes (CNTs) are added into a mixture of concentrated nitric acid and sulfuric acid, which is then heated at 40?80? C. for 0.5?6 hours. Secondly, the surface-functionalized CNTs and polyvinyl butyral (PVB) are dispersed and dissolved, respectively, in organic solvents at a mass ratio of 1:0.2?1:4?8 to form homogeneous spinning solution, which is squeezed into water as shell liquid with water as core liquid at a flow rate ratios of 0.5?5:1 through a spinneret to form CNT/PVB hollow fibers. Finally, the dry fibers are calcinated at 600?1000 ? C. for 1?4 hours in absence of oxygen to produce free-standing CNT hollow fiber membranes. The method involved in this invention is simple and highly efficient without needing any templates, expensive apparatuses and chemicals. Additionally, the obtained electrically conductive CNT hollow fiber membranes feature a high porosity, high water flux and strong acid/alkali resistance.

A method is disclosed for preventing carbon nanotube degradation in ionizable environments. The method includes immersing a porous thin-film nanotube (CNT)/polymer composite Joule heating element in an ionizable environment; and applying an alternating current at a frequency of at least 100 Hz to the porous thin-film nanotube (CNT)/polymer composite Joule heating element in the ionizable environment.

A carbon-dioxide-reducing film includes, an electrically conductive material, a carbon-dioxide adsorbent, and a proton-permeable high-molecular-weight material. The electrically conductive material includes at least one selected from a group consisting of carbon nanotubes, nanographenes, and carbon paper.