Carbon nanotube (CNT) is a prominent material for gas separation due to its inherent smoothness of walls, allowing rapid transport of gases compared to other inorganic fillers. It also possesses high mechanical strength, enabling membranes to operate at high pressure. Although it has superior properties compared to other inorganic fillers, preparation of CNTs into a polymer matrix remains challenging due to the strong van der Waals forces of CNTs, which lead to agglomeration of CNTs. To utilize the full potential of CNTs, proper dispersion of CNTs must be addressed. In this paper, methods to improve the dispersion of CNTs using functionalization methods were discussed. Fabrication techniques for CNT mixed-matrix membrane (MMM) nanocomposites and their impact on gas separation performance were compared. This paper also reviewed the applications and potential of CNT MMMs in gas separation.

In this work, in situ polymerization of modified sol-gel silica in a polyether sulfone matrix is presented to control the interfacial defects in organic-inorganic composite membranes. Polyether sulfone polymer and modified silica are used as organic and inorganic components of mixed matrix membranes (MMM). The membranes were prepared with different loadings (2, 4, 6, and 8 wt.%) of modified and unmodified silica. The synthesized membranes were characterized using Field emission electron scanning microscopy, energy dispersive X-ray, Fourier transform infrared spectroscopy, thermogravimetric analyzer, and differential scanning calorimetry. The performance of the membranes was evaluated using a permeation cell set up at a relatively higher-pressure range (5–30 bar). The membranes appear to display ideal morphology with uniform distribution of particles, defect-free structure, and absence of interfacial defects such as voids and particle accumulations. Additionally, the CO₂/CH₄ selectivity of the membrane increased with the increase in the modified silica content. Further comparison of the performance indicates that PES/modified silica MMMs show a promising feature of commercially attractive membranes. Therefore, tailoring the interfacial morphology of the membrane results in enhanced properties and improved CO₂ separation performance.

Ionic liquid mixed matrix membranes (IL3Ms) were synthesized using polyethersulfone (PES) as the base polymer and silica-aluminophosphate (SAPO-34) as the dispersed particles, and their CO₂ permeation was investigated. Three of the most widely used models for gas separation—the Maxwell, Lewis–Nielson, and Maxwell–Wagner–Sillar (MWS) models—were then applied to the membranes. Large deviations were found between the model predictions and experimental data. FESEM images suggested that local agglomeration and disorientation of the SAPO-34 particles within the membrane afforded substantial changes in the morphology. The MWS model, which considers the shape factor, was modified to incorporate the volume fraction of the wetted dispersed phase and the ideal shape factor. A direct relationship was found between the filler concentration and the shape factor. The modified model was shown to produce absolute and relative errors of less than 3%. When validated against data from the literature, the deviation remained within 5%. The modified model can be used to estimate the gas permeance of an IL3M.

Different compositions of carbon molecular sieve (CMS) were incorporated in polyethersulfone (PES) matrix to fabricate mixed matrix membranes (MMMs) by solution casting method. The characterization was carried out using field emission scanning electron microscopy (FESEM) analysis to investigate the morphology of membrane. FESEM images showed acceptable contacts between the filler particles and the polymer chains. The performance of the developed membrane is analyzed by single gas permeation measurement of high purity CO₂ and CH₄. Both CO₂ permeance and CO₂/CH₄ selectivity increased with CMS loadings as compared to pure PES membrane. Experimental results showed that the highest value of CO₂ permeance (66.71 GPU) and CO₂/CH₄ selectivity (10.94) can be achieved with 30 wt. % loading of CMS particles. This can be credited to size discrimination of CMS pores that falls between CO₂ and CH₄ kinetic diameters.