Nanostructured Membranes Research Articles

Self-assembled nanostructured membranes with tunable pore size and shape from plant-derived materials.

Nanostructured materials derived from sustainable sources are of interest as viable alternatives to traditional petroleum-derived sources in membrane applications due to environmental concerns. Here, we present the development of pore size-tunable nanostructured polymer membranes based on a plant-derived material. The membranes were fabricated using a tri-functional amine as the templating core species and a cross-linkable ligand synthesized from rose oil-derived citronellol. The self-assembly of a supramolecular complex between the template core and the ligand forms a hexagonally packed columnar (Colh) mesophase, the dimensions of which can be precisely controlled by changing the stoichiometric ratio between these constituents. Within the hexagonal mesophase stoichiometric range, the pore size of the nanostructured membranes can be tuned from 1.0 to 1.3 nm, with a step size of approximately 0.1 nm. The membranes exhibited a clear distinction in molecular size selectivity, as demonstrated by dye adsorption experiments. The membrane fabricated with a ligand-to-core ratio of 3 to 1 demonstrated shape-based selectivity, exhibiting a higher permeability for propeller-shaped penetrants and highlighting its potential for shape-selective transport. We anticipate that this straightforward approach, using plant-derived materials, can contribute to important sustainability aspects while enhancing the performance of current state-of-the-art nanostructured membranes by enabling precise control over pore size.

Selective O2-to-H2O2 Electrosynthesis by a High-Performance, Single-Pass Electrofiltration System Using Ibuprofen-Laden CNT Membranes.

Producing H2O2 through a selective, two-electron (2e) oxygen reduction reaction (ORR) is challenging, especially when it serves as an advanced oxidation process (AOP) for cost-effective water decontamination. Herein, we attain a 2e-selectivity H2O2 production using a carbon nanotube electrified membrane with ibuprofen (IBU) molecules laden (IBU@CNT-EM) in an ultrafast, single-pass electrofiltration process. The IBU@CNT-EM can generate H2O2 at a rate of 25.62 mol gCNT-1 h-1 L-1 in the permeate with a residence time of 1.81 s. We demonstrated that an interwoven, hydrophilic-hydrophobic membrane nanostructure offers an excellent air-to-water transport platform for ORR acceleration. The electron transfer number of the ORR for IBU@CNT at neutral pH was confirmed as 2.71, elucidating a near-2e selectivity to H2O2. Density functional theory (DFT) studies validated an exceptional charge distribution of the IBU@CNT for the O2 adsorption. The adsorption energies of the O2 and *OOH intermediates are proportional to the H2O2 selectivity (64.39%), higher than that of the CNT (37.81%). With the simple and durable production of H2O2 by IBU@CNT-EM electrofiltration, the permeate can actuate Fenton oxidation to efficiently decompose emerging pollutants and inactivate bacteria. Our study introduces a new paradigm for developing high-performance H2O2-production membranes for water treatment by reusing environmental functional materials.

Optimization of Reactive Ink Formulation for Controlled Additive Manufacturing of Copolymer Membrane Functionalization.

Multifunctional, nanostructured membranes hold immense promise for overcoming permeability-selectivity trade-offs and enhancing membrane durability in challenging molecule separations. Following the fabrication of copolymer membranes, additive manufacturing technologies can introduce reactive inks onto substrates to modify pore wall chemistries. However, large-scale implementation is hindered by a lack of systematic optimization. This study addresses this challenge by elucidating the membrane functionalization mechanisms and optimal manufacturing conditions using a copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) "click" reaction. Leveraging a data science toolkit (e.g., nonlinear regression, uncertainty quantification, identifiability analyses, model selection, and design of experiments), we developed two mathematical models: (1) algebraic equations to predict equilibrium concentrations after preparing reactive inks by mixing copper sulfate, ascorbic acid (AA), and an alkynyl-terminated reactant; and (2) reaction-diffusion partial differential equations (PDEs) to describe the functionalization process. The ink preparation chemistry with side reactions was validated through pH and UV-vis measurements, while the diffusion and kinetic parameters in the PDE model were calibrated using time-series conversion of the azide moieties inferred from Fourier-transform infrared spectroscopy. This modeling framework avoids redundant experimental efforts and offers a functionalization protocol for scaling up designs. Ink optimization problems were proposed to reduce the use of expensive and environmentally insulting ink materials, i.e., Cu(II), while ensuring the desired chemical distributions. With optimal ink formulation Cu(II)/AA/alkyne = 1:1:2 identified, we uncovered trade-offs between Cu(II) usage and functionalization time; for example, in continuous roll-to-roll manufacturing with a conserved functionalization bath setup, our optimal operational conditions to achieve ≥90% functionalization enable at least a 20% reduction in total copper investment compared to previous experimental results. The data science-enabled ink optimization framework is extendable for on-demand multifunctional membranes in numerous future applications such as metal recovery from wastewater and brine.

Fabrication of Nanofiber Membranes from Waste-Expanded Polystyrene (EPS) Combined with Zinc Oxide Nanoparticles (ZnO NPs) and its Photocatalytic Activity

Society must face the challenge of creating high-value products from recycled waste polymers. This research focuses on the synthesis of nanofiber membranes from waste-expanded polystyrene (EPS) using electrospinning. Zinc oxide nanoparticles (ZnO NPs) enhance the photocatalytic activity of the fiber membrane. ZnO is a more useful alternative to TiO2 as a form of photocatalyst for degrading contaminants in water. This study systematically investigated the effects of varying amounts of ZnO NPs on fiber membrane nanostructure and photocatalytic activity. Methylene blue was used to measure the photocatalytic efficiency of fiber membranes, as they are commonly used in textile wastewater and exposed to ultraviolet light for 20 h. The results showed that the fiber membrane containing ZnO NPs with a concentration of 1 % effectively degraded methylene blue. HIGHLIGHTS The EPS/ZnO nanofiber produced using electrospinning was characterized using SEM-EDX, FTIR, and Raman spectroscopy UV-Vis spectrophotometer testing proves that the EPS/ZnO nanofiber has photocatalytic activity capabilities that can remove organic contaminants The EPS/ZnO 1 % shows the highest efficiency; 45 % of methylene blue was degraded within 20 h of irradiation GRAPHICAL ABSTRACT

Scalable Purification, Storage, and Release of Plant-Derived Nanovesicles for Local Therapy Using Nanostructured All-Cellulose Composite Membranes.

Plant-derived nanovesicles such as bilberries nanovesicles (BNVs) show immense promise as next-generation biotherapeutics and functional food ingredients; however, their isolation, purification, and storage on a large scale remain a challenge. In this study, biocompatible and nanostructured composite all-cellulose membranes are introduced as a scalable and straightforward approach to the isolation of BNV. The membranes consisting of a cellulose acetate matrix infused with anionic or cationic nanocelluloses promoted selective capture of BNVs through electrostatic and size-exclusion-mediated depth filtration. Furthermore, the surface of the composite membrane acted as a storage matrix for BNVs, ensuring their prolonged stability at 4 °C. The BNVs stored in the membrane could be promptly released through elution assisted by low-pressure vacuum filtration or diffusion in liquid media. The morphology, bioactivity, and stability of the extracted BNVs were preserved, and the release rate of BNVs in different cell cultures could be regulated, facilitating their use for local therapy. Consequently, this approach paves the way for the scalable production, purification, and storage of nanovesicles and advances their use in biotherapeutics and functional foods.

Fabrication of Coffee‐Ring Nanostructured Membranes for Organic Solvent Nanofiltration

AbstractOrganic solvent nanofiltration (OSN) plays important roles in pharmaceutical ingredients purification and solvent recovery. However, the low organic solvent permeance under cross‐flow operation of OSN membrane hampers their industrial applications. Herein, we report the construction of coffee‐ring structured membrane featuring high OSN permeance. A water‐insoluble crystal monomer that dissolved in EtOH/H2O mixed solvent was designed to react with trimesoyl chloride via interfacial polymerization. Owing to the diffusion of EtOH to n‐hexane, coffee‐ring nanostructure on the support membrane appeared, which served as the template for construction of coffee‐ring structured membrane. The optimal nanostructured membrane demonstrated 2.6‐fold enhancement in the effective surface area with reduced membrane thickness. Resultantly, the membrane afforded a 2.7‐fold enhancement in organic solvent permeance, e.g., ~13 LMH/bar for MeOH, without sacrificing the rejection ability. Moreover, due to the rigid monomer structure, the fabricated membrane shows distinctive running stability in active pharmaceutical ingredients purification and the ability for concentration of medicines.

Fabrication of Coffee-Ring Nanostructured Membranes for Organic Solvent Nanofiltration.

Organic solvent nanofiltration (OSN) plays important roles in pharmaceutical ingredients purification and solvent recovery. However, the low organic solvent permeance under cross-flow operation of OSN membrane hampers their industrial applications. Herein, we report the construction of coffee-ring structured membrane featuring high OSN permeance. A water-insoluble crystal monomer that dissolved in EtOH/H2O mixed solvent was designed to react with trimesoyl chloride via interfacial polymerization. Owing to the diffusion of EtOH to n-hexane, coffee-ring nanostructure on the support membrane appeared, which served as the template for construction of coffee-ring structured membrane. The optimal nanostructured membrane demonstrated 2.6-fold enhancement in the effective surface area with reduced membrane thickness. Resultantly, the membrane afforded a 2.7-fold enhancement in organic solvent permeance, e.g., ~13 LMH/bar for MeOH, without sacrificing the rejection ability. Moreover, due to the rigid monomer structure, the fabricated membrane shows distinctive running stability in active pharmaceutical ingredients purification and the ability for concentration of medicines.

Development of superhydrophobic and superoleophilic CNT and BNNT coated copper meshes for oil/water separation

In this research, chemical vapor deposition (CVD) method was used to synthesize boron nitride nanotube (BNNT) powder. This method involves heating multi-walled carbon nanotube (MWCNT) and boric acid in the presence of ammonia gas up to 1000 °C. Then MWCNT and synthetic BNNT were coated on the copper mesh via dip-coating method separately to prepare nano-structured membranes for efficient oil/water separation. Various analyzes were performed to identify the synthetic BNNT properties (X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET), field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS) and prepared coated membranes (FESEM, atomic force microscopy (AFM), water contact angle (WCA), oil contact angle (OCA) and oil/water separation process). Water and oil contact angle analyzes showed the super-oleophilic properties of both membranes with the underwater OCA of about 128°. For the separation process, a dead-end filtration setup was used, and free oil water mixture and o/w emulsion were prepared. So, in the separation process water was retained and decalin passed through both prepared membranes. The flux of CNT coated membrane was about 458 L m2 h−1, while this amount was 1834 L m2 h−1 for BNNT coated membrane and 99% separation efficiency was achieved by both of them. This four-fold increase in flux is due to the fact that the inner diameter of boron nitride nanotubes synthesized is four times larger than the inner diameter of MWCNT.

Chemical nature evolution of solid supports used in electromembrane extraction procedures: A comparative analysis based on metric tools

BackgroundIn recent decades, green chemistry has been focusing on the adaptation of different chemical methods towards environmental friendliness. Sample preparation procedures, which constitute a fundamental step in analytical methodology, have also been modified and implemented in this direction. In particular, electromembrane extraction (EME) procedures, which have traditionally used plastic supports, have been optimized towards greener approaches through the emergence of alternative materials. In this regard, biopolymer-based membranes (such as agarose or chitosan) have become versatile and very promising substitutes to perform these processes. ResultsDifferent green metric tools (Analytical Eco-Scale, ComplexGAPI and AGREEprep have been applied to study the evolution of solid supports used in EME from nanostructured tissues and polymer inclusion membranes to agar films and chitosan flat membranes. The main goal is to evaluate the usage of these new biomaterials in the analytical procedure to quantify their environmental impact in the frame of Green Analytical Chemistry (GAC). In addition, both RGB model and BAGI metrics have been employed to study the sustainability of the whole procedure, including not only greenness, but also analytical performance and feasibility aspects. Results obtained after the performance of the mentioned metrics have demonstrated that the most efficient and environmentally friendly analytical methods are based on the use of chitosan supports. This improvement is mainly due to the chemical nature of this biopolymer as well as to the removal of organic solvents. SignificanceThis work highlights the advantages of biodegradable materials employment in EME procedures to achieve green analytical methodologies. These materials also contribute to raise the figure of merits regarding to the quantification parameters in a wide range of applications compared to classical supports employed in EME, thus enhancing sustainability of procedures.

Combined antibacterial and antifouling properties of polyethersulfone mixed matrix membranes with zwitterionic graphene oxide nanostructures

AbstractThe impact of zwitterionic graphene oxide (GO‐Arg) nanostructures into polyethersulfone (PES) membranes was studied, aiming to perform mixed matrix membranes (MMMs) with combined antibacterial and antifouling properties. For this purpose, 0.25, 0.50, and 1.0 wt% of GO‐Arg were incorporated through the phase inversion method. The chemical composition reveals that the electrostatic interactions of PES, polyvinylpyrrolidone, and GO‐Arg occur by enhancing the CH/NH vibrations associated with the intrinsic MMMs and their combined antibacterial and antifouling performance. Well‐defined finger‐like morphology was observed, performing the pore distribution and the finger‐cavity inclination induced by the electrostatic charge of GO‐Arg. As a result, GO‐Arg MMM's hydrophobic properties decreased from 77.8° to 52.3°, inducing a partially hydrophilic surface and improved water flux. The isoelectric point of nanostructured membranes slightly changes by the charge modulation produced by zwitterionic GO‐Arg. The antibacterial activity against Gram (−) Escherichia coli was improved, closing the complete bacterial inhibition after 24 h. As a result, antifouling performance was improved, avoiding bacterial adhesion into the membrane surface and the possibility of promoting biofilm formation. Our results demonstrate that zwitterionic nanomaterials in MMMs perform the multifunctional capacity of materials, emerging as an effective alternative with potential application in wastewater treatment.Highlights The incorporation of zwitterionic GO‐Arg improves the mechanical properties of MMMs. GO‐Arg‐enhanced well‐defined porous finger‐like morphology in MMMs. GO‐Arg improves the antibacterial/antifouling performance of PES‐based MMMs.

Enhancement of acoustic properties of carbon fibrous membrane (CFM) by in-situ crystallization of PZT nanogenerators (PENGs) inside the fibers for a low-frequency acoustic energy harvesting

Acoustic energy harvesting (AEH) by a nanostructured membrane has recently gained increasing attention. This study focused on a novel approach for in-situ crystallization of Pb(Zr0.58Ti0.42)O3 (PZT) as a piezoelectric nanogenerator (PENG) inside the carbon fibrous membranes (CFM). The electrospinning process and post-heat treatment were applied to synthesize the CFM-embedded PENG, which benefits from both the flexibility of carbon fibers and the piezoelectric properties of the crystallized PZT. The results indicated that the carbon fibers kept their microstructure over the heat treatment at 250 and 350 °C while the crystallization fraction of PZT increased. The XPS analysis revealed that the CFM embedded by in-situ crystallized PENG had a higher diversity of tetragonal and rhombohedral in comparison with the CFM embedded by the pre-crystallized PENGs. Furthermore, the electrical conductivity, dielectric constant, and ferromagnetic properties of CFM were improved with the incorporation of the in-situ crystallized PENGs. The acoustic studies in the range of 250–2000 Hz under sound pressure of 90 dB revealed that sound absorption performance of CFM was increased by about +35 %. Also, the ability of CFM in the AEH process was enhanced drastically by embedding the PENGs inside the carbon fibers. The maximum harvested electricity at 500 Hz was 5.9 and 13.9 W m−2 by CFM embedded by in-situ crystallized and pre-crystallized PENGs, respectively. The above results exhibit the great potential for the CFM-embedded PENGs to be used in low-frequency AEH applications.

Theoretical study on symmetric and asymmetric stacking in the self-assembly of bola-amphiphilic peptides into membranes with mixtures of EF4E and KF4K

In this work, we conducted a study on peptide membranes formed by the amino acid sequences EF4E and KF4K with the aim of obtaining energetic and structural results for asymmetric and symmetric membrane nanostructures. The results show that the lifetime of hydrogen bonds (HBs) for peptides in the symmetric membrane is ∼12 % higher than that observed for the asymmetric structure, providing greater rigidity to the former. These findings are consistent with those obtained for Coulomb and van der Waals interaction energies and demonstrate that the Symmetric model exhibits better stability compared to the Asymmetric model. The average thickness of the membranes is ∼1.72 ± 0.06 nm and ∼2.27 ± 0.02 nm for the asymmetric and symmetric models, respectively. Our results show that the symmetric model stands out due to greater structural organization and consequently a less hydrated appearance in the membrane region, which could be crucial for applications. From an electrical perspective, both membranes display clear differences, underscoring the influence of peptide arrangement on the membrane structure.

Nanofiltration membrane with surface nanostructure induced by interfacial modification for heavy metal ions removal, salt selection and antibacterial

Positively charged nanofiltration membranes offer promising options for the removal of heavy metal ions. However, their electrical properties often lead to serious drawbacks such as impaired filtration performance and poor fouling resistance, thus further modification of these positively charged membranes are imperative. Herein, we report the interfacial manipulation of nanofiltration membranes using a hydroxyl monomer (β-cyclodextrin) in concert with the typical positively charged ammonia monomer (polyethyleneimine) to achieve efficient removal of heavy metals, improved perm-selectivity and fouling resistance. The results indicated that water flux of the modified membrane was increased by over 2-folds owing to structural modification compared with pristine membrane. The charge effects and enhanced cross-linking improve the rejection of salts ions, especially divalent ions. The topological and Turing-structured membranes reached 99.9% removal of heavy metal ions due to the combination of adsorption, complexation, Donnan and site resistance effects, and has excellent stability. Additionally, the functionalized membranes exhibited reduced adhesion and survival of bacteria on the surface based on the excellent bacteriostatic and hydrophilicity properties. These findings revealed the mechanism of interfacial modification induction on the nanostructure and properties of membranes and provided an efficient solution for the synthesis of multifunctional membranes.

Photon-Induced Near-Field Electron Microscopy of Nanostructured Metallic Films and Membranes

Photon-Induced Near-Field Electron Microscopy of Nanostructured Metallic Films and Membranes

Rational engineering WO3-X/CNTs@carbon fiber membrane for the high-efficient produce H2O2 via electrochemical two-electron water oxidation route

The electrochemical two-electron water oxidation reaction (2e-WOR) offers a promising avenue for hydrogen peroxide (H2O2) production. It is crucial to design electrocatalysts with high selectivity, yield, resource abundance, and environmental friendliness. In this paper, as a new generation 2e-WOR electrocatalyst, the WO3-X/CNTs@carbon fiber membrane nanostructure with abundant oxygen-rich vacancy (OV) has been discovered by a series of test techniques including XRD, FE-SEM, TEM, FT-IR, Raman and XPS, comprising interconnected carbon nanotubes and carbon fibers enveloped in WO3 nanorods with oxygen-rich vacancies. By comparing the specific surface area of WO3-x/CNTs@carbon fiber membrane at different temperatures, it was observed that the maximum value is 44.09 m2/g when the mass ratio of AMT to PAN was 3:2 at 600 °C. Furthermore, the WO3-X/CNTs@carbon fiber membrane can be directly utilized as an independent electrode. The electrochemical performance test revealed that the Faraday efficiency of the WO3-X/CNTs @CF-600-2 can reach 54 % (2.48 V vs RHE (reversible hydrogen electrode)), while the H2O2 yield can achieve 10.3 μmol· min−1·cm−2, nearly ten times higher than that of pure WO3. Furthermore, the stability testing demonstrated that after 12 h, the WO3-X/CNTs @CF-600-2 exhibited excellent stability with minimal change in its Faraday efficiency. This enhancement is attributed to the improved selectivity of WO3, excellent electrical conductivity, and mass transfer performance of carbon fiber. Finally, we proposed a mechanism for 2e-WOR and provided some perspectives on this reaction along with summarizing recent discoveries.

In Vivo Validation of a Nanostructured Electrospun Polycaprolactone Membrane Loaded with Gentamicin and Nano-Hydroxyapatite for the Treatment of Periodontitis.

The aim of this research was to validate the use of a gentamicin (GEN) and nano-hydroxiapatite (nHAP)-loaded polycaprolactone nanostructured membrane (NM) as an innovative, highly efficient, low-cost treatment for periodontitis. We conducted an in vivo study on Wistar rats, in which we induced periodontitis by placing silk ligatures around the first right and left upper molars. The subjects were divided into three groups; the first group received no periodontal treatment, the second group received open flap debridement, and the third group received open flap debridement, together with the positioning of the GEN and nHAP-loaded nanostructured membrane as a treatment. The extent of periodontal regeneration was assessed by the periodontal pocket depth, bleeding on probing, tooth mobility, dental plaque, microbiological analysis, concentration of MMP-8 in saliva, plasma levels of CRP, and histological analysis. The results showed that using open flap debridement with the NM is more efficient, and it significantly reduces the probing depth, extent of bleeding on probing, dental mobility, bacterial plaque, and pathogenic flora. The concentrations of MMP-8 and CRP decrease. The histological analysis demonstrated that NM leads to bone regeneration. Our study indicates that gentamicin and nano-hydroxyapatite embedded in the fiber of the biodegradable membranes might be a promising therapeutic option for periodontitis treatment.

Recent advances and applications of nanostructured membranes in water purification.

In recent years, water pollution caused by hazardous materials such as metals, drugs, pesticides, and insecticides has become a very serious environmental and health problem that needs to be addressed urgently. The nutritional needs associated with the increasing population also increase the demand for water use and rapidly increase the rate of freshwater consumption. Since most of the water in the universe is in the form of sea water, which cannot be directly used, freshwater resources are limited, compared to the existing available water. When addressing the purification of all kinds of pollution in environmental research, nanostructured membranes attract attention as alternative solutions for water treatment. Nanostructured membranes, which can be used for filtration and water treatment process, are summarized in recent research. Various types of nanostructured membranes are presented and used to remove salts and metallic ions in water treatment processes. The representations and application areas of these membrane systems are explained. Consequently, new water treatment nanostructured membranes that can be developed and their effective separation performances are described. The benefits of nanostructured membranes for water treatment and their progress in purification are discussed.

Real-time simultaneous refractive index and thickness mapping of sub-cellular biology at the diffraction limit

Mapping the cellular refractive index (RI) is a central task for research involving the composition of microorganisms and the development of models providing automated medical screenings with accuracy beyond 95%. These models require significantly enhancing the state-of-the-art RI mapping capabilities to provide large amounts of accurate RI data at high throughput. Here, we present a machine-learning-based technique that obtains a biological specimen’s real-time RI and thickness maps from a single image acquired with a conventional color camera. This technology leverages a suitably engineered nanostructured membrane that stretches a biological analyte over its surface and absorbs transmitted light, generating complex reflection spectra from each sample point. The technique does not need pre-existing sample knowledge. It achieves 10−4 RI sensitivity and sub-nanometer thickness resolution on diffraction-limited spatial areas. We illustrate practical application by performing sub-cellular segmentation of HCT-116 colorectal cancer cells, obtaining complete three-dimensional reconstruction of the cellular regions with a characteristic length of 30 μm. These results can facilitate the development of real-time label-free technologies for biomedical studies on microscopic multicellular dynamics.

Suspension electrospinning of SBR latex combined with photo-induced crosslinking: control of nanofiber composition, morphology, and properties

Suspension electrospinning of a styrene-butadiene rubber (SBR) latex coupled with photo-induced crosslinking in ambient conditions is proposed as a rapid method to prepare ultrafine shape-stable rubber fibrous membranes. Polyethylene oxide (PEO) is used as template polymer and can eventually be removed from the nanostructured membrane by a simple water treatment. A multifunctional thiol crosslinker and an appropriate photo-initiating system are added to the latex to allow the fast and efficient photo-induced crosslinking of the nanofibers, based on thiol addition to the SBR double bonds, as demonstrated by real-time Infrared spectroscopy analyses. It is proved that by varying the PEO template polymer and the thiol crosslinker content, a fine control of the chemical composition, morphology, water solubility, and thermal properties of the nanofibrous membranes is ensured. Moreover, comparable mechanical properties to those of fibrous membranes produced by conventional electrospinning of organic solvent-based solutions are obtained, clearly showing the attractiveness of the present method, especially in terms of process sustainability.Graphical abstract

Addressing challenges with evaluating hydrogen-selective membrane performance by quadrupole mass spectrometry.

Hydrogen separation using nanostructured membranes has gained research attention because of its potential to produce high-purity hydrogen by separating gases at the molecular level. Quadrupole mass spectrometry (QMS) is one method to evaluate these membranes' effectiveness in separating hydrogen from gas mixtures. However, quantifying gases in a mixture with QMS is challenging, especially when heavier gas ions interfere with a light gas ion, resulting in lower quantification accuracy. This study addresses this challenge by presenting a detailed calibration procedure that significantly improves hydrogen quantification accuracy up to a factor of 2.5. CO and CO2 were chosen as interfering gases because they are commonly released in conventional hydrogen production processes. By carefully evaluating the performance of these membranes, new opportunities for hydrogen separation may be realized.