Search Results (7)

This study investigated the enhancement in bioethanol recovery from mixed matrix membranes (MMMs) by functionalizing zeolite framework-8 (ZIF-8) with imidazolate. This study focused on the separation of ethanol from low-concentration ethanol/water mixtures (typical post-fermentation concentrations of 5–10 wt%). Specifically, ZIF-8 was modified by the shell–ligand exchange reaction (SLER) with 5,6-dimethylbenzimidazole (DMBIM), resulting in ZIF-8-DMBIM particles with improved hydrophobicity, organophilicity, larger size, and adjustable pore size. These particles were incorporated into a PEBAX 2533 matrix to produce ZIF-8-DMBIM/PEBAX MMMs using a dilution blending method. The resulting membranes showed significant performance enhancement: 8 wt% ZIF-8-DMBIM loading achieved a total flux of 308 g/m²·h and a separation factor of 16.03, which was a 36.8% increase in flux and 176.4% increase in separation factor compared with the original PEBAX membrane. In addition, performance remained stable during a 130 h cycling test. These improvements are attributed to the enhanced compatibility and dispersion of ZIF-8-DMBIM in the PEBAX matrix. In conclusion, the evaluation of nanofiller content, feed concentration, operating temperature, and membrane stability confirmed that ZIF-8-DMBIM/PEBAX MMM is ideal for ethanol recovery in primary bioethanol concentration processes. Full article

Novel composite membranes employing a poly(ether-block-amide) (PEBAX) copolymer and sulfonated montmorillonite (S-MMT) as a filler were developed. The ratio of polyether to polyamide blocks was investigated using PEBAX 2533 and PEBAX 4533 based on the membrane properties and performance. Additionally, the effect of the changing filler ratio was monitored. The interaction between the S-MMT as nanofiller and the polymer matrix of PEBAX2533 and PEBAX4533 as well as the crystalline nature and thermal and mechanical stability of the composite membranes were evaluated using Fourier Transform Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and tensile test. The composite membrane with 7 wt.% S-MMT showed the highest water uptake of 21% and 16% and an acceptable swelling degree of 16% and 9% for PEBAX 2533 and PEBAX 4533 composite membranes, respectively. In terms of water uptake and ion exchange capacity at room temperature, the new un-protonated membranes are superior to un-protonated Nafion. Meanwhile, with the same S-MMT content, the ion conductivity of PEBAX 2533 and PEBAX 4533 composite membranes is 2 and 1.6 mS/cm, and their ion exchange capacity is 0.9 and 1.10 meq/g. Full article

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. Full article

In this study, we mixed the zeolitic imidazolate framework-7 (ZIF-7) with poly(ether-b-amide)^® 2533 (Pebax-2533) and used it as a selective layer for a composite membrane. We prepared the composite membrane’s substrate using polysulfone (PSf), adjusted its pore size using polyethylene glycol (PEG), and applied polydimethylsiloxane (PDMS) to the gutter layer and the coating layer. Then, we investigated the membrane’s properties of gases by penetrating a single gas (N₂, CO₂) into the membrane. We identified the peaks and geometry of ZIF-7 to determine if it had been successfully synthesized. We confirmed that ZIF-7 had a BET surface area of 303 m²/g, a significantly high Langmuir surface area of 511 m²/g, and a high CO₂/N₂ adsorption selectivity of approximately 50. Considering the gas permeation, with ZIF-7 mixed into Pebax-2533, N₂ permeation decreased from 2.68 GPU in a pure membrane to 0.43 GPU in the membrane with ZIF-7 25 wt%. CO₂ permeation increased from 18.43 GPU in the pure membrane to 26.22 GPU in the ZIF-7 35 wt%. The CO₂/N₂ ideal selectivity increased from 6.88 in the pure membrane to 50.43 in the ZIF-7 25 wt%. Among the membranes, Pebax-2533/ZIF-7 25 wt% showed the highest permeation properties and the characteristics of CO₂-friendly ZIF-7. Full article

Membrane separation technology can used to capture carbon dioxide from flue gas. However, plenty of research has been focused on the flat sheet mixed matrix membrane rather than the mixed matrix thin film hollow fiber membranes. In this work, mixed matrix thin film hollow fiber membranes were fabricated by incorporating amine functionalized UiO-66 nanoparticles into the Pebax^® 2533 thin selective layer on the polypropylene (PP) hollow fiber supports via dip-coating process. The attenuated total reflection-Fourier transform infrared (ATR-FTIR), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX) mapping analysis, and thermal analysis (TGA-DTA) were used to characterize the synthesized UiO-66-NH₂ nanoparticles. The morphology, surface chemistry, and the gas separation performance of the fabricated Pebax^® 2533-UiO-66-NH₂/PP mixed matrix thin film hollow fiber membranes were characterized by using SEM, ATR-FTIR, and gas permeance measurements, respectively. It was found that the surface morphology of the prepared membranes was influenced by the incorporation of UiO-66 nanoparticles. The CO₂ permeance increased along with an increase of UiO-66 nanoparticles content in the prepared membranes, while the CO₂/N₂ ideal gas selectively firstly increased then decreased due to the aggregation of UiO-66 nanoparticles. The Pebax^® 2533-UiO-66-NH₂/PP mixed matrix thin film hollow fiber membranes containing 10 wt% UiO-66 nanoparticles exhibited the CO₂ permeance of 26 GPU and CO₂/N₂ selectivity of 37. Full article

In this work, the behavior of new GO-based mixed matrix membranes was tested in view of their use as CO₂-selective membrane in post combustion carbon capture applications. In particular, the new materials were obtained by mixing of Pebax^® 2533 copolymer with different types of graphene oxide (GO). Pebax^® 2533 has indeed lower selectivity, but higher permeability than Pebax^® 1657, which is more commonly used for membranes, and it could therefore benefit from the addition of GO, which is endowed with very high selectivity of CO₂ with respect to nitrogen. The mixed matrix membranes were obtained by adding different amounts of GO, from 0.02 to 1% by weight, to the commercial block copolymers. Porous graphene oxide (PGO) and GO functionalized with polyetheramine (PEAGO) were also considered in composites produced with similar procedure, with a loading of 0.02%wt. The obtained films were then characterized by using SEM, DSC, XPS analysis and permeability experiments. In particular, permeation tests with pure CO₂ and N₂ at 35°C and 1 bar of upstream pressure were conducted for the different materials to evaluate their separation performance. It has been discovered that adding these GO-based nanofillers to Pebax^® 2533 matrix does not improve the ideal selectivity of the material, but it allows to increase CO₂ permeability when a low filler content, not higher than 0.02 wt%, is considered. Among the different types of GO, then, porous GO seems the most promising as it shows CO₂ permeability in the order of 400 barrer (with an increase of about 10% with respect to the unloaded block copolymer), obtained without reducing the CO₂/N₂ selectivity of the materials, which remained in the order of 25. Full article

Membrane technology can be used for both post combustion carbon dioxide capture and acidic gas sweetening and dehydration of natural gas. These processes are especially suited for polymeric membranes with polyether functionality, because of the high affinity of this species for both H₂O and CO₂. Here, both crosslinked polyethylene glycol diacrylate and a polyether-polyamide block copolymer (PEBAX 2533^©) are studied for their ability to separate CO₂ from CH₄ and N₂ under single and mixed gas conditions, for both dry and wet feeds, as well as when 500 ppm H₂S is present. The solubility of gases within these polymers is shown to be better correlated with the Lennard Jones well depth than with critical temperature. Under dry mixed gas conditions, CO₂ permeability is reduced compared to the single gas measurement because of competitive sorption from CH₄ or N₂. However, selectivity for CO₂ is retained in both polymers. The presence of water in the feed is observed to swell the PEG membrane resulting in a significant increase in CO₂ permeability relative to the dry gas scenario. Importantly, the selectivity is again retained under wet feed gas conditions. The presence of H₂S is observed to only slightly reduce CO₂ permeability through both membranes. Full article