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.

The present invention pertains to a porous membrane, to a process for manufacturing said porous membrane and to use of said porous membrane as filtration membrane for liquid and/or gas phases, in particular water-based phases.

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 method for preparing a resin-treated microporous membrane by electrodeposition is disclosed.

The present invention relates to shaped bodies comprising a composition (Z1), wherein said composition comprises at least one polymer having an elongation at break of >30% and at least one porous metal-organic framework material, to processes for producing shaped bodies of this kind and to the use of a composition (Z1) comprising at least one polymer having an elongation at break of >30% and at least one porous metal-organic framework material for production of a film, membrane or laminate having a water vapor permeability according to DIN 53122 at 38? C./90% rel. humidity of greater than 1000 g/(m.sup.2*d), based on a film thickness of 10 ?m.

A membrane based process separates amines or organic acids from a solution containing at least one amine or at least one organic acid according to their hydrophobic properties. The more hydrophobic amine or organic acid passes the hydrophobic membrane into an acidic aqueous solution, thus selectively removing the amine or organic acid from the first solution. The process is particularly suitable to obtain chiral amines in high yield. A transaminase-catalyzed transamination of an amino donor and amino acceptor is combined with a hydrophobic membrane separation of the produced chiral amine. The selective removal of the chiral amine from the reaction mixture promotes the further transformation of the amino acceptor into the product chiral amine.

The invention provides a porous membrane comprising polyvinyl chloride (PVC) and at least one inorganic filler embedded in the porous membrane wherein the inorganic filler comprises sulfuric acid precipitated silica. The invention further provides a process for the production of said porous membrane.

The present invention relates to a method to synthesize ammonia at moderate conditions. The present invention also relates to a new chemical reactor configuration to achieve ammonia synthesis at moderate pressures and temperatures, and methods to make membranes for use in ammonia synthesis.

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.

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.