A facile method for separating fine water droplets dispersed in oil through a pre-wetted mesh membrane.

To achieve the successful separation of emulsions containing fine dispersed droplets and low volume fractions, a membrane with pore sizes comparable to or smaller than the droplet size is typically required. Although this approach is effective, its utilization is limited to the separation of emulsions with relatively large droplets. To overcome this limitation, a secondary membrane can be formed on the primary membrane to reduce pore size, but this can also be time-consuming and costly. Therefore, a facile and effective method is still required to be developed for separating emulsions with fine droplets. We introduce a pre-wetted mesh membrane with a pore size significantly larger than droplets, easily fabricated by wetting a hydrophilic stainless-steel mesh with water. Applying this membrane to emulsion separation via gravity-driven flow confirms a high efficiency greater than 98%, even with droplets approximately 10 times smaller than the pore size.

Synthesis of Aluminum-Based Metal-Organic Framework (MOF)-Derived Carbon Nanomaterials and Their Water Adsorption Isotherm.

The characteristics of water vapor adsorption depend on the structure, porosity, and functional groups of the material. Metal-organic framework (MOF)-derived carbon (MDC) is a novel material that exhibits a high specific area and tunable pore sizes by exploiting the stable structure and porosity of pure MOF materials. Herein, two types of aluminum-based MOFs were used as precursors to synthesize hydrophobic microporous C-MDC and micro-mesoporous A-MDC via carbonization and activation depending on the type of ligands in the precursors. C-MDC and A-MDC have different pore characteristics and exhibit distinct water adsorption properties. C-MDC with hydrophobic properties and micropores exhibited negligible water adsorption (108.54 mgg-1) at relatively low pressures (P/P0~0.3) but showed a rapid increase in water adsorption ability (475.7 mgg-1) at relative pressures of about 0.6. A comparison with the isotherm model indicated that the results were consistent with the theories, which include site filling at low relative pressure and pore filling at high relative pressure. In particular, the Do-Do model specialized for type 5 showed excellent agreement.

Asymmetric Supercapacitors Using Porous Carbons and Iron Oxide Electrodes Derived from a Single Fe Metal-Organic Framework (MIL-100 (Fe)).

MOF-derived carbon (MDC) and metal oxide (MDMO) are superior materials for supercapacitor electrodes due to their high specific capacitances, which can be attributed to their high porosity, specific surface area (SSA), and pore volume. To improve the electrochemical performance, the environmentally friendly and industrially producible MIL-100 (Fe) was prepared using three different Fe sources through hydrothermal synthesis. MDC-A with micro- and mesopores and MDC-B with micropores were synthesized through carbonization and an HCl washing process, and MDMO (α-Fe2O3) was obtained by a simple sintering in air. The electrochemical properties in a three-electrode system using a 6 M KOH electrolyte were investigated. These novel MDC and MDMO were applied to an asymmetric supercapacitor (ASC) system to overcome the disadvantages of traditional supercapacitors, enhancing energy density, power density, and cyclic performance. High SSA materials (MDC-A nitrate and MDMO iron) were selected for negative and positive electrode material to fabricate ASC with KOH/PVP gel electrolyte. As-fabricated ASC resulted in high specific capacitance 127.4 Fg-1 at 0.1 Ag-1 and 48.0 Fg-1 at 3 Ag-1, respectively, and delivered superior energy density (25.5 Wh/kg) at a power density 60 W/kg. The charging/discharging cycling test was also conducted, indicating 90.1% stability after 5000 cycles. These results indicate that ASC with MDC and MDMO derived from MIL-100 (Fe) has promising potential in high-performance energy storage devices.

Hydrogen molecules trapped in interstitial host channels of alpha-hydroquinone.

Easy come, easy go: Hydroquinone forms a channel structure of cages with hydrogen-bonded hexagons. These may provide an ideal route for the fast inclusion and facile release of hydrogen molecules (see figure), which can lead to reversible hydrogen storage under mild conditions.

Critical guest concentration and complete tuning pattern appearing in the binary clathrate hydrates.

The concept of tuning phenomenon in binary hydrate systems has been suggested to enhance the gas storage capacity through molecular interactions. In this report, the existence of critical guest concentration (CGC) is investigated by means of spectroscopic methods. The existence of the critical guest concentration can act as a limiting factor in the application areas of binary hydrates. Therefore, it should be taken into account before applying this concept to application fields. In addition, further research on this concept using other hydrate systems is required to clarify the present findings.

Tuning clathrate hydrates for hydrogen storage.

The storage of large quantities of hydrogen at safe pressures is a key factor in establishing a hydrogen-based economy. Previous strategies--where hydrogen has been bound chemically, adsorbed in materials with permanent void space or stored in hybrid materials that combine these elements--have problems arising from either technical considerations or materials cost. A recently reported clathrate hydrate of hydrogen exhibiting two different-sized cages does seem to meet the necessary storage requirements; however, the extreme pressures (approximately 2 kbar) required to produce the material make it impractical. The synthesis pressure can be decreased by filling the larger cavity with tetrahydrofuran (THF) to stabilize the material, but the potential storage capacity of the material is compromised with this approach. Here we report that hydrogen storage capacities in THF-containing binary-clathrate hydrates can be increased to approximately 4 wt% at modest pressures by tuning their composition to allow the hydrogen guests to enter both the larger and the smaller cages, while retaining low-pressure stability. The tuning mechanism is quite general and convenient, using water-soluble hydrate promoters and various small gaseous guests.