A hydrophilic graphitic material is provided that may be formed by heating a graphitic material to a temperature between about 150° C. to about 1400° C. for an extended period of time under an inert atmosphere. Annealing CNT film at 500 to 1400 removes amorphous carbon to produce purified CNT film. The purified CNT film can be further densified with the treatment of alkylphosphonic acid or alkyldiphophonic acid and heating to produce a hydrophilic, densified CNT film which is mechanically robust and does not adhere to other solid surfaces. These films can be used as filtration membranes with superior membrane fouling resistance among other uses.

The present disclosure relates to a phenyl-modified polydimethylsiloxane (PDMS) separation membrane, a fabrication method thereof, and a use thereof in the separation of an aromatic compound, and belongs to the technical field of separation membrane materials. A phenyl-modified PDMS separation membrane comprising a substrate layer and a selective layer is provided.

A membrane modification method for improving liquid membrane separation of carbon dioxide (CO.sub.2) includes grafting an organic substance containing an amine group on a porous membrane material, and loading water into pore channels of the porous membrane material to prepare a supported liquid membrane for a gas mixture separation experiment of CO.sub.2. In the method, the amine group is introduced through chemical grafting to make the water being alkaline when used as membrane liquid. Compared with an alkaline solution as the membrane liquid, the method can avoid the loss of active alkaline substances and increase the permeation flux of CO.sub.2.

Provided is a porous hollow fiber membrane made of a thermoplastic resin, wherein a membrane thickness is 0.050 mm or larger and 0.25 mm or smaller, and when a strength coefficient is defined as K=(compressive strength)/((membrane thickness)/(inside diameter/2)).sup.3, K=1.7 or more.

The present invention relates to a separator membrane having a hierarchical structure, a production method therefor and a xylene separation method using same, and to: a separator membrane having a hierarchical structure comprising mesopores, the separator membrane having mesopores introduced inside a microporous zeolite separator membrane, thereby being thin, having less defects and exhibiting high xylene permeation and separation performance; a production method therefor; and a xylene separation method using same.

Disclosed are a light-driven filtration antibacterial composite membrane and a preparation method and use thereof. The method for preparing the light-driven filtration antibacterial composite membrane includes: mixing dichloromethane and N,N-dimethylformamide to obtain a first solution; adding PCL particles to the first solution, and stirring until being uniform to obtain an electrospinning solution; adding a ZIF-8 powder to the electrospinning solution, and ultrasonically dispersing for at least 1 hour to obtain a PCL/ZIF-8 spinning solution; spraying the PCL/ZIF-8 spinning solution onto a PPCL@PDA/TAEG men-blown membrane to obtain the light-driven filtration antibacterial composite membrane.

The present disclosure provides the synthesis of an imidazolium-based functional ionic liquid copolymer (PMMA-b-PIL-R*) and a preparation method of an alloy ultra-filtration membrane. Firstly, PMMA-b-PIL-R* is prepared from methyl methacrylate (MMA) and polymerizable imidazolium-based functional ionic liquid (IL-R*) containing double bonding as the reactive monomers through sequential radical polymerization. With the use of a non-solvent induced phase separation method, PMMA-b-PIL-R* is introduced into the body of a polymeric membrane material, so as to prepare an alloy ultra-filtration membrane. A hydrogen-bond interaction is generated between the carbonyl in the molecular chain of PMMA-b-PIL-R* and the H . . . C—Cl structure in the molecular chain of the polymeric membrane material, which enhances the compatibility between the molecular chains of PMMA-b-PIL-R* and the polymeric membrane material, so that it can be stable in the ultra-filtration membrane; the imidazole groups and functional groups in the molecular chain of PMMA-b-PIL-R* can provide a good hydrophilicity.

The present invention relates to a continuous process for preparing permselective hollow fiber membranes being suitable e.g. for hemodialysis, hemodiafiltration and hemofiltration of blood which comprises a two-stage drying and tempering treatment of the hollow fiber membranes. According to a further aspect, the invention relates to a continuous process for drying permselective hollow fiber membranes on-line. The invention also relates to devices for on-line drying of permselective hollow fiber membranes.

A composite membrane and moisture adjustment module using the same is disclosed. The composite membrane includes a moisture-permeable resin layer interposed between porous membranes that constitute a pair; and the mean thickness of the moisture-permeable resin layer is 5 μm or less.

The disclosure provides a method for preparing a hollow fiber membrane by melt spinning-stretching and selective swelling, including: preparing a nascent hollow fiber by melt spinning in an inert gas protective atmosphere by using an amphiphilic block copolymer as a film forming material, and stretching the nascent hollow fiber in the cooling process, a stretch rate being controlled at 200-540 mm/min, and a stretch ratio being controlled at 150-600%; immersing the obtained hollow fiber in a swelling solvent, and treating the hollow fiber in a water bath at 65° C. for 1 h; and then transferring the hollow fiber into a long-chain alkane solvent, treating the hollow fiber at the same temperature for 1-12 h, and after the completion of the treatment, immediately taking out the hollow fiber and drying the hollow fiber to obtain the hollow fiber membrane with a bicontinuous porous structure. By combining the melt spinning-stretching and the selective swelling, the method of the disclosure can synchronously and continuously improve the permeability and selectivity of the hollow fiber membrane. The treatment in the long-chain alkane solvent can make the polar chain excessively enriched on the surface of the membrane migrate inward, thereby improving the performance of the hollow fiber membrane.