A Drying-Free, Water-Based Process for Fabricating Mixed-Matrix Membranes with Outstanding Pervaporation Performance.

Despite much progress in the development of mixed matrix membranes (MMMs) for many advanced applications, the synthesis of MMMs without particle agglomeration or phase separation at high nanofiller loadings is still challenging. In this work, we synthesized nanoporous zeolitic imidazole framework (ZIF-8) nanoparticles with a particle size of 60 nm and a pore size of 0.34 nm in water and directly added them into an aqueous solution of the organic polymer poly(vinyl alcohol) (PVA) without an intermediate drying process. This approach led to a high-quality PVA/ZIF-8 MMM with enhanced performance in ethanol dehydration by pervaporation. The permeability of this MMM is three times higher than that of pristine PVA, and the separation factor is nearly nine times larger than that of pristine PVA. The significantly improved separation performance was attributed to the increase in the fractional free volume in the membranes.

Multilayered poly(vinylidene fluoride) composite membranes with improved interfacial compatibility: correlating pervaporation performance with free volume properties.

A spin-coating process integrated with an ozone-induced graft polymerization technique was applied in this study. The purpose was to improve the poor interfacial compatibility between a selective layer of poly(2-hydroxyethyl methacrylate) (PHEMA) and the surface of a poly(vinylidene fluoride) (PVDF) substrate. The composite membranes thus fabricated were tested for their pervaporation performance in dehydrating an ethyl acetate/water mixture. Furthermore, the composite membranes were characterized by field emission scanning electron microscopy (FE-SEM) for morphological change observation and by Fourier transform infrared spectroscopy equipped with attenuated total reflectance (ATR-FTIR) for surface chemical composition analysis. Effects of grafting density and spin-coating speed on pervaporation performance were examined. The composite membrane pervaporation performance was elucidated by means of free volume and depth profile data obtained with the use of a variable monoenergy slow positron beam (VMSPB). Results indicated that a smaller free volume was correlated with a higher pervaporation performance of a composite membrane consisting of a selective layer of spin-coated PHEMA on a PHEMA-grafted PVDF substrate (S-PHEMA/PHEMA-g-PVDF). The composite membrane depth profile illustrated that an S-PHEMA layer spin-coated at a higher revolutions per minute (rpm) was thinner and denser than that at a lower rpm.

Ultrathin graphene oxide-based hollow fiber membranes with brush-like CO2-philic agent for highly efficient CO2 capture.

Among the current CO2 capture technologies, membrane gas separation has many inherent advantages over other conventional techniques. However, fabricating gas separation membranes with both high CO2 permeance and high CO2/N2 selectivity, especially under wet conditions, is a challenge. In this study, sub-20-nm thick, layered graphene oxide (GO)-based hollow fiber membranes with grafted, brush-like CO2-philic agent alternating between GO layers are prepared by a facile coating process for highly efficient CO2/N2 separation under wet conditions. Piperazine, as an effective CO2-philic agent, is introduced as a carrier-brush into the GO nanochannels with chemical bonding. The membrane exhibits excellent separation performance under simulated flue gas conditions with CO2 permeance of 1,020 GPU and CO2/N2 selectivity as high as 680, demonstrating its potential for CO2 capture from flue gas. We expect this GO-based membrane structure combined with the facile coating process to facilitate the development of ultrathin GO-based membranes for CO2 capture.

Tuning nanostructure of graphene oxide/polyelectrolyte LbL assemblies by controlling pH of GO suspension to fabricate transparent and super gas barrier films.

A technique of layer-by-layer (LbL) self-assembly was used to prepare transparent multilayered gas barrier films consisting of graphene oxide (GO)/branched poly(ethylenimine) (BPEI) on a poly(ethylene terephthalate) substrate. The effect of the GO suspension pH on the nanostructure and oxygen barrier properties of the GO/BPEI film was investigated. The oxygen barrier properties of the assemblies were shown to be highly dependent on the pH. It was demonstrated that the film assemblies prepared using a GO suspension with a pH of 3.5 exhibited very dense and ordered structures and delivered very low oxygen transmission rates (the lowest was <0.05 cm(3) m(-2) day(-1)). The assemblies were characterized with ultraviolet-visible spectroscopy and ellipsometry to identify the film growth mechanism, and the result indicated a linear growth behavior. To analyze the nanostructure of the films, atomic force microscopy, transmission electronic microscopy, and grazing incidence wide-angle X-ray diffraction were used.