The Optimization of Dispersion and Application Techniques for Nanocarbon-Doped Mixed Matrix Gas Separation Membranes

In this work, supported cellulose acetate (CA) mixed matrix membranes (MMMs) were prepared and studied concerning their gas separation behaviors. The dispersion of carbon nanotube fillers were studied as a factor of polymer and filler concentrations using the mixing methods of the rotor–stator system (RS) and the three-roll-mill system (TRM). Compared to the dispersion quality achieved by RS, samples prepared using the TRM seem to have slightly bigger, but fewer and more homogenously distributed, agglomerates. The green γ-butyrolactone (GBL) was chosen as a polyimide (PI) polymer-solvent, whereas diacetone alcohol (DAA) was used for preparing the CA solutions. The coating of the thin CA separation layer was applied using a spin coater. For coating on the PP carriers, a short parameter study was conducted regarding the plasma treatment to affect the wettability, the coating speed, and the volume of dispersion that was applied to the carrier. As predicted by the parameter study, the amount of dispersion that remained on the carriers decreased with an increasing rotational speed during the spin coating process. The dry separation layer thickness was varied between about 1.4 and 4.7 μm. Electrically conductive additives in a non-conductive matrix showed a steeply increasing electrical conductivity after passing the so-called percolation threshold. This was used to evaluate the agglomeration behavior in suspension and in the applied layer. Gas permeation tests were performed using a constant volume apparatus at feed pressures of 5, 10, and 15 bar. The highest calculated CO2/N2 selectivity (ideal), 21, was achieved for the CA membrane and corresponded to a CO2 permeability of 49.6 Barrer.

Deep Eutectic Solvent-Functionalized Mesoporous Silica SBA-15-Based Mixed Matrix Polymeric Membranes for Mitigation of CO2

In this research, a novel DES (choline chloride + decanoic acid) was synthesized, and SBA-15 was functionalized by the DES to form a DES-SBA filler to fabricate MMMs. DES-SBA-based MMMs at 5%, 10%, 15%, and 20% were synthesized and evaluated. The DES-SBA-based MMMs were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). Gas permeation tests were applied to the pure and mixed gas samples, and the results of the permeability and selectivity (CO2/CH4, and CO2/N2) of the membranes are reported. DES modification of SBA-15 increased the efficiency of the synthesized MMMs in comparison with the pristine polysulfone membrane.

Tunning CO2 Separation Performance of Ionic Liquids through Asymmetric Anions

This work aims to explore the gas permeation performance of two newly-designed ionic liquids, [C2mim][CF3BF3] and [C2mim][CF3SO2C(CN)2], in supported ionic liquid membranes (SILM) configuration, as another effort to provide an overall insight on the gas permeation performance of functionalized-ionic liquids with the [C2mim]+ cation. [C2mim][CF3BF3] and [C2mim][CF3SO2C(CN)2] single gas separation performance towards CO2, N2, and CH4 at T = 293 K and T = 308 K were measured using the time-lag method. Assessing the CO2 permeation results, [C2mim][CF3BF3] showed an undermined value of 710 Barrer at 293.15 K and 1 bar of feed pressure when compared to [C2mim][BF4], whereas for the [C2mim][CF3SO2C(CN)2] IL an unexpected CO2 permeability of 1095 Barrer was attained at the same experimental conditions, overcoming the results for the remaining ILs used for comparison. The prepared membranes exhibited diverse permselectivities, varying from 16.9 to 22.2 for CO2/CH4 and 37.0 to 44.4 for CO2/N2 gas pairs. The thermophysical properties of the [C2mim][CF3BF3] and [C2mim][CF3SO2C(CN)2] ILs were also determined in the range of T = 293.15 K up to T = 353.15 K at atmospheric pressure and compared with those for other ILs with the same cation and anion’s with similar chemical moieties.

Poly(ethylene glycol) Diacrylate Iongel Membranes Reinforced with Nanoclays for CO2 Separation

Despite the fact that iongels are very attractive materials for gas separation membranes, they often show mechanical stability issues mainly due to the high ionic liquid (IL) content (≥60 wt%) needed to achieve high gas separation performances. This work investigates a strategy to improve the mechanical properties of iongel membranes, which consists in the incorporation of montmorillonite (MMT) nanoclay, from 0.2 to 7.5 wt%, into a cross-linked poly(ethylene glycol) diacrylate (PEGDA) network containing 60 wt% of the IL 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C2mim][TFSI]). The iongels were prepared by a simple one-pot method using ultraviolet (UV) initiated polymerization of poly(ethylene glycol) diacrylate (PEGDA) and characterized by several techniques to assess their physico-chemical properties. The thermal stability of the iongels was influenced by the addition of higher MMT contents (>5 wt%). It was possible to improve both puncture strength and elongation at break with MMT contents up to 1 wt%. Furthermore, the highest ideal gas selectivities were achieved for iongels containing 0.5 wt% MMT, while the highest CO2 permeability was observed at 7.5 wt% MMT content, due to an increase in diffusivity. Remarkably, this strategy allowed for the preparation and gas permeation of self-standing iongel containing 80 wt% IL, which had not been possible up until now.

The effects of cellulose nanofibers compounded in water-based undercoat paint on the discoloration and deterioration of painted wood products

Cellulose nanofibers (CNFs) have many potentials as filler to improve the properties of the other materials. We have developed the novel paints containing CNFs, and which controlled the discoloration of wood products. To clarify the discoloration mechanism of wood panels using an undercoat paint containing CNFs, prepared by an integrated process from Cryptomeria japonica, the composites and films made of CNFs and acryl resin that was a raw material for the paints were prepared. Observation of the surface of the CNFs/acryl resin composite film by atomic force microscopy showed that the fibers and the resin were uniformly mixed. The composite film prevented light transmittance in the ultraviolet (UV) light region, as well as oxygen gas permeation. The permeability coefficient of the oxygen gas decreased to 60% with the addition of 1.5 wt% of CNFs to the acryl resin. The addition of CNFs also increased the breaking stress by approximately 1.5 times compared with the acryl resin film. Electron spin resonance (ESR) analysis after UV irradiation resulted in the lowest radical formation of a piece of wood wrapped in the CNFs/acryl resin composite compared with the acryl-coated specimen and the wood as it was. Therefore, the CNFs composite film shielded the UV rays and oxygen more effectively than the original acryl resin, making it difficult for these factors to reach the wood’s surface, and thus, perhaps suppressing the generation of radicals from the wood. These actions would suppress the production of coloring substances caused by the radicals, resulting in the suppression of discoloration. Furthermore, the increase in the film’s strength by the addition of CNFs would have enhanced the stability of overall the paints with a CNF-containing undercoat. These effects might have contributed not only to the prevention of discoloration but also to the prevention of the occurrence of minute cracks caused by various weather deterioration factors.

Performance Evaluation of PDMS or PEBAX-Coated Polyetherimide Membrane for Oxygen/Nitrogen Separation

Since the industrial revolution era, the Earth was suffering from serious air pollution. Millions of people are now suffering from indoor air pollution related diseases, especially in the industrialized countries such as China. One method to improve the indoor air quality is by oxygen enhancement. Membrane technology has been a key research over the past decades due to its low energy usage, minimum chemical consumption as well as small setting up layout. In this study, polyetherimide (PEI) membranes coated with polydimethylsiloxane (PDMS) or poly(ether block amide) (PEBAX) at different concentration (1, 3 or 5 wt%) were used to evaluate the oxygen/nitrogen gas separation. Prior to the gas permeation study, the membranes were characterized using scanning electron microscope (SEM) for morphology observation and surface elemental analysis by energy dispersive X-ray spectroscope (EDX). The morphology of the self-fabricated PEI membranes is composed of a thin and dense structure supported by the finger-like structure. The results obtained from oxygen/nitrogen separation studies shows membrane coated with 3 wt% PDMS yield a good separation results, exhibiting an improvement of oxygen and nitrogen permeance by 28.2% and 24.9%, selectivity by 10.4% (up to 5.08) relative to the base PEI membrane. Meanwhile, the 3 wt% PEBAX-coated PEI membrane only achieved selectivity of 3.56. The PDMS-coated PEI membrane yield a better separation performance attributed to the fact that PDMS coating on the hollow fiber membrane improve the surface morphology by reducing the defects.

Membrane Separation of Gaseous Hydrocarbons by Semicrystalline Multiblock Copolymers: Role of Cohesive Energy Density and Crystallites of the Polyether Block

The energy-efficient separation of hydrocarbons is critically important for petrochemical industries. As polymeric membranes are ideal candidates for such separation, it is essential to explore the fundamental relationships between the hydrocarbon permeation mechanism and the physical properties of the polymers. In this study, the permeation mechanisms of methane, ethane, ethene, propane, propene and n-butane through three commercial multiblock copolymers PEBAX 2533, PolyActive1500PEGT77PBT23 and PolyActive4000PEGT77PBT23 are thoroughly investigated at 33 °C. This study aims to investigate the influence of cohesive energy density and crystallites of the polyether block of multiblock copolymers on hydrocarbon separation. The hydrocarbon separation behavior of the polymers is explained based on the solution–diffusion model, which is commonly accepted for gas permeation through nonporous polymeric membrane materials.

Polymeric Membrane for CO2/CH4 Separation

This chapter presents a critical overview of polymeric membrane applications for CO2/CH4 separation. Comparative summary of availability and practice of different gas separation methods are outlined to give a state-of-the-art view of this technology. Detailed discussions on polymer-based membranes are also discussed in this work, highlighting the mechanism of selective gas permeation through the membranes. Future direction is discussed for possible new experimental design to maximize the membrane performances in separation of CO2/CH4.