An apparatus and method for transferring nanofiber structures (e.g., nanofiber films, nanofiber sheets, stacks of nanofiber grids, nanofiber films, nanofiber sheets, and combinations thereof) between various substrates are described. The techniques described use a soluble layer on a substrate that is subsequently dissolved, thus freeing the nanofiber structure from the substrate. This liquid phase techniques preserves the mechanical integrity and the purity of the nanofiber structures.

A method for preparation of conductive polymer/carbon nanotube (CNT) composite nanofiltration (NF) membrane and the use thereof. This conductive polymer/CNT composite NF membrane is obtained by polymerizing conductive polymer into a CNT membrane and then in-situ cross-linking with glutaraldehyde under acidic condition. The synthetic method for the conductive polymer/CNT composite NF membrane is simple and has no need of expensive equipment. The prepared membrane has controllable membrane structure and possesses superior electrical conductivity and electrochemical stability. The membrane can couple with electrochemistry for electrically assisted filtration. With the electrical assistance, the membrane can achieve improved ion rejection performance while retaining high permeability by enhancement of membrane surface charge density, which alleviates the permeability-selectivity trade-off. Furthermore, the electrically assisted NF membrane filtration can also enhance the removal for small molecular organic pollutants.

Embodiments described herein relate generally to durable graphene oxide membranes for fluid filtration. For example, the graphene oxide membranes can be durable under high temperatures non-neutral pH, and/or high pressures. One aspect of the present disclosure relates to a filtration apparatus comprising: a support substrate, and a graphene oxide membrane disposed on the support substrate. The graphene oxide membrane has a first lactose rejection rate of at least 50% with a first 1 wt % lactose solution at room temperature. The graphene oxide membrane has a second lactose rejection rate of at least 50% with a second 1 wt % lactose solution at room temperature after the graphene oxide membrane is contacted with a solution that is at least 80° C. for a period of time.

The present invention provides a multi-stage filter system suitable for the production of drinking water from a wide variety of contaminated water sources. The modular nature of the multi-stage filter system allows for the customization of filter combinations according to the remediation requirements. The multi-stage filter system comprises a coarse filter (S1); an ultrafiltration filter (S2); a graphene-based filter (S3); and a residual nanoparticle filter (S4). The graphene-based filter cartridge comprises few-layer graphene powder; a combination of few-layer graphene powder and pellets comprising a mixture of polyethersulfone, graphene oxide (GO), and dimethylformamide; a composite comprising chitosan, GO, sodium sulfate and ferric chloride; or a combination of few-layer graphene powder, granular activated carbon and a composite comprising chitosan, GO, sodium sulfate and ferric chloride.

Solar electroosmosis power generation devices and methods thereof are disclosed. In some embodiments, a first electrode in transparent inorganic electrolyte solution is provided in a first temperature chamber including a first light-transmitting wall. A second electrode in transparent inorganic electrolyte solution is provided in a second temperature chamber including a second light-tight wall. The first and second temperature chambers are connected by a cation nano-film with nanoparticles on its surface close to the first temperature chamber. An external circuit connects the first and second electrodes. When the nano-film is irradiated through the first wall by sunlight, the temperature of the first temperature chamber is higher than that of the second temperature chamber. In some embodiments, the solar electroosmosis power generation device improves solar energy utilization efficiency, and can be used in the field of solar light-heat-electric conversion.

A hybrid membrane, particularly of polyacrylonitrile (PAN)/graphene oxide (GO)/SiO.sub.2, separates oil and water even from emulsions. The membrane can be made by one-step electrospinning, adding GO and SiO.sub.2 nanofillers in PAN in various concentrations. The nanofillers may be uniformly embedded in the nanofibrous structure of the electrospun hybrid membrane, with GO mainly embedded inside the PAN nanofibers and may cause knots, and/or SiO.sub.2 nanoparticles embedded on the nanofiber surface and may form micro-nano fiber surface protrusions. Hierarchical structures formed can have enhanced hydrophilicity due to oxygen-containing groups on both SiO.sub.2 and GO, and have >99% oil rejection from oil-water emulsions. Separation flux and phase rejection of gravity separation may be enhanced by incorporation of nanofillers, which may also enhance membrane mechanical properties. Separated water flux may be enhanced from 2600 (pure PAN) to 3151 Lm.sup.−2h.sup.−1 for the hybrid.

A filter unit includes an inlet for receiving unfiltered water. A first fluid path directs water through a membrane and a filter element to a first outlet. Additionally, a second fluid path directs water across the membrane and to a second outlet.

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.

A process for preparing a microcapillary carbon molecular sieve membrane may include extruding a polyvinylidene chloride polymer to a thickness from 10 μm to 1,000 μm to form an extruded polymeric microcapillary film, wherein the extruded polymeric microcapillary film comprises a first end, a second end, and one or more microcapillaries extending from the first end to the second end; pre-treating the extruded polymeric microcapillary film at a temperature from 100° C. to 200° C. for a time from 1 hour to 48 hours to form a pre-treated polymeric microcapillary film; and pyrolizing the pre-treated polymeric microcapillary film at a temperature from 200° C. to 1,500° C. for a time from 15 minutes to 5 hours to form the microcapillary carbon molecular sieve membrane.

The disclosure is directed to a device that includes an upper container configured to receive a fluid sample collected from a mammal into a first opening, the first opening opposite a second opening and a membrane covering at least a portion of the second opening, the membrane configured to allow transmission of a portion of the fluid sample through the membrane.