Microstructure Of Membranes Research Articles

Deep learning-assisted prediction and profiled membrane microstructure inverse design for reverse electrodialysis

Compared to traditional inter-membrane spacers, profiled ion exchange membranes significantly improve the energy harvesting performance of reverse electrodialysis (RED). Here computational fluid dynamics is employed to generate data regarding the flow and mass transfer characteristics and performance index under different profiled membrane microstructures. Data-driven deep learning models are constructed for microstructure shape generation, physics field prediction, and performance forecasting. Results show that the microstructure shape generation via the Bezier generative adversarial network, the physical field prediction via conditional generative adversarial network for the velocity field and the performance prediction via multi-layer perceptron for power number and Sherwood number achieves satisfied accuracy, respectively. The gradient descent algorithm is utilized to optimize the microstructure shape achieving higher mass transfer performance and lower pump power consumption. Compared to the traditional straight ridge channel, the optimized microstructure channel exhibits a reduction of 18.85 % in the power number and an increase of 41.00 % in the Sherwood number, rendering significantly boosted performance.

Enhanced Organic Solvent Nanofiltration Membranes with Double Permeance via Laser‐Induced Graphitization of Polybenzimidazole

AbstractThis study investigates the fabrication of organic solvent nanofiltration (OSN) membranes through laser‐induced graphitization of polybenzimidazole (PBI). Employing a CO2 laser, the polymer is converted into graphene, resulting in controlled submicron‐scale porous 3D structures, a feat not achievable with traditional methods such as chemical crosslinking. The effectiveness of this process hinges on precise adjustments of laser parameters, such as fluence, to attain the ideal graphitization levels. The findings indicate that partial graphitization, as opposed to excessive, is crucial for preserving the membrane's microstructure and enhancing its functional properties. The partially graphitized PBI‐LIG (Polybenzimidazole ‒ Laser‐induced Graphene) membranes achieved up to 94% rejection of Congo red from ethanol, with an ethanol permeance rate of 12.14 LMH bar−1—nearly twice that of standard PBI membranes. Additionally, these membranes showcased outstanding chemical stability and solvent resistance, maintaining over 99% structural integrity and experiencing <1% weight loss after prolonged exposure to various industrial solvents over a week. These results highlight the potential of laser‐graphitized PBI membranes for applications in harsh chemical conditions, paving the way for further optimization of high‐performance OSN membranes. This research advances membrane technology, merging laser engineering with materials science, and contributes to environmental sustainability and industrial efficiency.

Quaternized poly(aryl imidazolium) containing bulky binaphthyl group as proton exchange membrane for high-temperature fuel cells

The low power output and high phosphoric acid (PA) leakage are the main constraints restricting the commercialization of PA-doped high-temperature proton exchange membranes (HT-PEMs). Ionized imidazoles have been shown to be an effective strategy to improve PA retention, however, less research has been conducted on the fractional free volume (FFV) of the backbone of the main chain on PA loss. Herein, novel imidazolium ions polymer (PQBN-4-IM) material with bulky binaphthyl (BN) group was prepared as PA-doped HT-PEM using a one-step superoxid acid catalyzed polycondensation and subsequent methylation process. The rigidity and hydrophobicity of the BN group promote PQBN-4-IM PEM to produce more obvious microphase separation morphology and large FFV, which is beneficial for forming better ion transport channels and excellent PA interaction. Notably, the PA-doped PQBN-4-IM (PQBN-4-IM/PA) membrane has the highest proton conductivity (90.26 mS cm−1, 180 ℃) and peak power density (PPD) (802.5 mW cm−2, 180 ℃) than PQTP-4-IM/PA and m-PBI/PA HT-PEMs. Moreover, the PQBN-4-IM/PA membrane has higher PA retention at 80 ℃/40 % relative humidity (RH), 40 ℃/60 % RH, or immersed in water due to enhancement on ion-pair interactions by microstructure. Under the accelerated stress test (AST) of the fuel cell (FC), the PQBN-4-IM/PA membrane loses only 12.22 % of PPD after 200 cycles at 80 ℃, which exhibits higher PPD retention than that of the PQBP-4-IM/PA (70.23 %), PQTP-4-IM/PA (74.36 %) and m-PBI/PA (65.25 %) membranes, and shows excellent durability of cell performance for more than 1000 h without significant voltage decay at 160 °C. Thus, the outstanding performance suggests that the microstructure and morphology of imidazolium ions polymer membranes significantly influence proton conductivity, performance, and the durability of a cell.

The role of one-dimensional materials in modulating the selective mass transport of covalent organic framework membranes for nanofiltration

Two-dimensional covalent organic frameworks (2D COFs) membranes have well-ordered nanochannels for selective molecular sieving. One-dimensional (1D) materials have been proposed to link the loosely packed COFs nanosheet for enhancing the separation performance of COFs membranes. However, it remains unclear how the enhancement arises. Herein, we demonstrate the role of 1D materials in modulating the microstructure and interlayer force of 2D COFs membranes. The optimized composite membrane, assembled from 2D COFs and chitosan exhibits a 75% enhancement in permeance without sacrificing selectivity towards different dyes. Our results show that the interaction forces between COFs and 1D materials are directly correlated to the transport nanochannels. When the interaction forces are stronger, the microstructure is more densely packed. Meanwhile, the shielding effect of 1D materials on the intrinsic channels of 2D COFs is more significant, resulting in narrow transport channels for mass transfer. In contrast, the weaker interaction forces prevent the excessive shrinkage of nanochannels, facilitating fast mass transfer and maintaining the high molecular selectivity. The work unravels the interaction forces between 2D COFs and 1D materials leading to the shaping of mass transfer nanochannels, offering a new perspective for the advancement of COFs membrane for nanofiltration.

Effect of N-isopropylacrylamide and graphene oxide on the microstructure and performance of thermo-responsive membranes by Ce (IV)-induced redox radical polymerization

In this study, a series of novel thermo-responsive materials were synthesized using polyvinylidene fluoride, N-isopropylacrylamide (NIPAM) and graphene oxide (GO) via Ce (IV)-induced redox radical polymerization name as PNG. Thermo-responsive membranes were prepared by non-solvent induced phase separation. The results demonstrated that the CO and N-H stretching absorption intensities increased with the addition of NIPAM. XPS analysis demonstrated that the PNG1 membrane exhibited abundant functional group structure under the dosage of NIPAM at 1 g. The finger-like porous structure of membrane became longer and wider with the addition of NIPAM at 1 g, leading to a maximum porosity of 45.5 %. The CA decreased from 62.4 ° to 49.0 ° at 35 °C under the adding dosage of NIPAM at 1 g. The temperature-sensitive of PNG1 membrane was 35 °C. In addition, The PNG1 membrane had the lower Rir and higher flux recover than the others under the BSA rejection. According to the XDLVO theory analysis, the total interaction energy for PNG1 membrane achieved the maximum absolute values of −33.850 mJ/m2 and −19.956 mJ/m2 than the others under the temperature at 25 °C and 35 °C. This interaction influenced the adsorption between the pollutant and membrane surface, resulting in reversible fouling.

Exploring of novel reverse thermally induced phase separation process based on preparation and characterization of polysulfate ultrafiltration membranes with bicontinuous structure

AbstractContaminated water sources from various industries pose severe environmental challenges due to their complex compositions, high toxicity, and fluctuating qualities. This study introduces a groundbreaking strategy for fabricating advanced polysulfate (PSE) ultrafiltration membranes using a novel reverse thermally induced phase separation (RTIPS) process. By manipulating the cloud point through the DMAc/DEG solvent/nonsolvent system, our work innovatively controls membrane microstructure, overcoming limitations of conventional nonsolvent‐induced phase separation (NIPS). Our findings reveal that RTIPS, when employed above the cloud point, yields PSE membranes with a unique bicontinuous sponge‐like structure, significantly improving upon conventional NIPS products. Specifically, the optimized RTIPS membranes exhibit enhanced pure water flux (916.23 vs. 336.23 LMH), larger pore sizes (0.083 vs. 0.054 μm), increased tensile strength (1.32 vs. 0.84 MPa), and improved fouling resistance (FRR 65.5% vs. 55.2%). This research pioneers a facile yet potent method for tailoring membrane properties, achieving a balance between permeability, mechanical stability, and filtration efficacy. The demonstrated success of RTIPS in enhancing PSE membrane performance not only contributes to the development of high‐performance water treatment technologies but also charts a new course in membrane science, offering a promising avenue for sustainable wastewater management solutions.

Highly selective thin B-oriented MFI zeolite membranes on scalable modified stainless steel supports

Enhancing the separation performance of molecular sieve membranes relies significantly on precise control over their membrane morphology and microstructure. This involves creating thin, closely packed, oriented, and uniform coatings of seed crystals, enabling subsequent intergrowth to establish continuous membranes. To address industrial needs, it is crucial to generate a thin and flawless membrane efficiently producible on a large-scale support. Porous stainless supports offer scalability and easy integration into membrane modules. In this study, we present a novel and straightforward process for modifying stainless-steel supports to seed zeolite membrane layers. High-performance, b-oriented MFI zeolite membranes can be synthesized on these modified stainless-steel supports through scalable filtration seeding of MFI zeolite nanosheets followed by secondary growth. By employing a carefully designed pre-treatment procedure, we achieved the growth of well-intergrown, highly b-oriented MFI zeolite membranes on the modified stainless-steel support, establishing a robust interaction with the substrate. The membranes, fabricated through gel-free secondary growth of nanosheets deposited on a scalable stainless-steel support using this technique, demonstrate ultra-selective capabilities in separating para-xylene from ortho-xylene, with a high separation factor of 388.

Solar/microwave-driven composite membrane evaporation and its application in seawater desalination

Increased economic growth and population expansion has heightened the demand for water resources, leading to escalating levels of water scarcity. Sustainable seawater desalination methods, powered by renewable energy, offer promising solutions to the long-standing global water shortage. This study presents a method for seawater desalination that employs eco-friendly materials. The approach involves utilizing metakaolin-based porous geopolymer (GP) as the base material, and depositing graphene oxide (GO) to create a graphene oxide geopolymer (GOGP) composite membrane. The membrane undergoes in-situ self-reduction to obtain reduced graphene oxide geopolymer (rGOGP). The study examines the composition, microstructure, and water evaporation performance of the composite membrane under both solar/microwave-driven. The results show that, under microwave conditions with a frequency of 2450 MHz and power of 400 W, the evaporation rate can reach up to 4.13 kg·m−2·h−1, doubling the evaporation rate achieved through solar-driven evaporation at an equivalent efficiency level. Furthermore, the evaporation rate of the composite membrane remains consistent when exposed to high-concentration saltwater of 15 wt%. Notably, the removal rates of Na+, K+, Ca2+, and Mg2+ all exceed 99 %, meeting the drinking water requirements established by the World Health Organization. This study provides a novel approach to seawater desalination utilizing environmentally friendly materials and clean energy sources.

Sandwich-structured electrospun polyvinylidene difluoride sensor for structural health monitoring of glass fiber reinforced polymer composites

Stress monitoring and interlaminar failure detection attract much attention in glass fiber reinforced polymer (GFRP) structural health monitoring area. However, due to limitations of sensing or electrode materials, existing embedding sensors cannot be designed to have both of the abilities without sacrificing mechanical properties. This work fabricated a sandwich-structured sensor, which is composed of three layers of electrospun polyvinylidene difluoride membranes. The upper and lower electrodes are flexible membranes that ensure stable signal collection in the rigid GFRP material system. The sensor can quantitatively monitor the stress based on piezoelectric effect, and interlaminar crack propagation based on parallel plate capacitors. The voltage and capacitance values have a linear relationship with the stress level and crack length (R-square of the functions is 0.999 and 0.933), respectively. Due to the porous microstructure of electrospun membranes, polymer matric can well infiltrate the polyvinylidene difluoride nanofibers while preparing the sensor embedded GFRP. Thus, the perfect bonding of the sensor within GFRP ensures the effective sensing abilities until sample failure and negligible effect (< -7%) on the mechanical properties of GFRP.

Improved purification efficiency and stability of photocatalytic cement-based pavement coated with colloidal graphitic carbon nitride

Photocatalytic coatings applied onto cement-based pavement materials have been intensely developed to purify runoff pollution and vehicle exhaust. However, the masking effect of the adhesive incorporation often results in an unsatisfactory purification efficiency. Thus, developing an adhesive-free photocatalytic coating with high stability and purification efficiency on cement-based pavements is still urgently needed. Herein, a colloidal graphitic carbon nitride (g-C3N4) modified with hydroxyl groups was sprayed onto cement pastes to prepare a photocatalytic coating on the cement-based materials. The results of photocatalytic degradation of Rhodamine B (RhB) indicated that the RhB degradation efficiency and stability of the colloidal g-C3N4-coated cement paste were significantly improved compared to pristine g-C3N4-coated cement paste. After a runoff-washing trial, photocatalytic RhB degradation by colloidal g-C3N4-coated cement paste was 13.8-fold higher than that of pristine g-C3N4-coated cement paste. Mechanistic studies suggested that the well-distributed membrane microstructure of colloidal g-C3N4 and coordinate bonds between colloidal g-C3N4 and calcium-silicate-hydrates were mainly responsible for the improved stability and purification efficiency of colloidal g-C3N4-coated cement pastes. These results support the use of colloidal g-C3N4 as a promising strategy to prepare photocatalytic cement-based pavements with good stability and purification efficiency.

Titania and zirconia ceramic nanofiltration membrane fabrication by coating method on mullite and mullite-alumina microfiltration supports for industrial wastewater treatment

Industrial wastewater treatment increasingly relies on membrane separation, with ceramic membranes offering many advantages such as thermal stability and pH resistance. The resistance of ceramic membranes to extreme pH conditions indicates their ability to maintain structure and performance when exposed to highly acidic or alkaline environments. A high-permeability ceramic nanofiltration membrane was developed, boasting excellent rejection rates through a multilayer asymmetric design. Initially, two tubular porous supports, mullite and mullite-alumina, with a weight percent of 50, were fabricated using the extrusion method. Subsequently, a colloidal sol of titania (TiO2) and titania-zirconia (TiO2- ZrO2) was prepared via the sol–gel method and coated on the ceramic supports using the dip-coating method. After analyzing the membrane microstructure using SEM, XRD, and BET, the efficiency of the membranes in treating synthetic oily wastewater was evaluated. The results underscore the significant impact of the Donnan exclusion mechanism on the rejection of nanofiltration (NF) membranes. An increase in pressure led to a rise in rejection rates up to 7 bars. The Chemical Oxygen Demand (COD) rejection for mullite-titania zirconia (MTZ) and mullite-alumina-titania zirconia (MATZ) membranes was 98.65 % and 98 %, respectively. The pure water permeability test results for mullite and mullite-alumina supports, as well as MTZ and MATZ membranes, were recorded as 254, 382, 70, and 89 L bar-1m-2h−1, respectively.

Mechanistic insights into the separation behaviors of polyamide desalination membranes for emerging micropollutants removal

As emerging micropollutants (EMPs) become a global environmental concern, it is crucial to devise energy-efficient methods that can effectively remove EMPs from water. Polyamide thin-film composite (PA-TFC) membranes are state-of-the-art water separation membranes and their applications for EMPs separations have been increasingly conscripted in recent years. However, a comprehensive fundamental understanding of the underlying relationship between membrane microstructures and EMPs transport across the PA-TFC membranes remains enigmatic. To address this gap, we thoroughly investigated the separation behaviors of two PA-TFC membranes with distinct PA microstructures toward a wide spectrum of EMPs with various dimensions and chemistries. By reconciling experimental evidence and density-functional theory (DFT), we disclosed that the water permeance of the PA-TFC membrane is predominately governed by the effective filtration area associated with surface protuberances and the intrinsic wall thickness of the PA microlayers. Precise control of the solute–PA interactions is explicitly important for membrane selectivity toward EMPs, which deserves more attention in future membrane design besides synchronously regulating membrane pore size and size distribution. This work represents a conspicuous step forward in the fundamental understanding of the structure–performance relationship of PA-TFC membranes for EMPs separations, which would inspire the rational construction and structural regulation of high-performance membranes for new pollutants removal.

Impact of Nonsolvent–Solvent Affinity on Membrane Morphology and Microstructure: Unraveling the Transition from Traversing Pore to Closed Void Structures

Impact of Nonsolvent–Solvent Affinity on Membrane Morphology and Microstructure: Unraveling the Transition from Traversing Pore to Closed Void Structures

Fullerene in Water Remediation Nanocomposite Membranes—Cutting Edge Advancements

Among carbon nanoparticles, fullerene has been observed as a unique zero-dimensional hollow molecule. Fullerene has a high surface area and exceptional structural and physical features (optical, electronic, heat, mechanical, and others). Advancements in fullerene have been observed in the form of nanocomposites. Application of fullerene nanocomposites has been found in the membrane sector. This cutting-edge review article basically describes the potential of fullerene nanocomposite membranes for water remediation. Adding fullerene nanoparticles has been found to amend the microstructure and physical features of the nanocomposite membranes in addition to membrane porosity, selectivity, permeation, water flux, desalination, and other significant properties for water remediation. Variations in the designs of fullerene nanocomposites have resulted in greater separations between salts, desired metals, toxic metal ions, microorganisms, etc. Future investigations on ground-breaking fullerene-based membrane materials may overcome several design and performance challenges for advanced applications.

Understanding interfacial polymerization in the formation of polyamide RO membranes by molecular simulations

Since the water permeation mechanisms of polyamide membranes are highly dependent on the micro-structure of polyamide membranes, a deeper understanding of the formation process of them is necessary for the optimization of the membrane performance. As most simulation works construct the polyamide membranes in an ideal way, the interfacial diffusion of monomers, which is crucial for the formation of polyamide membranes, is usually ignored. To address this issue, we mimic the experimental conditions to develop an atomic model of a highly crosslinked polyamide membrane by conducting molecular dynamics simulations. Via tuning the concentration and molar ratio of monomers, the diffusion of monomers and its influence on the subsequent reaction are altered, and the final membrane structure consequently changed. Simulation results reveal that increasing the trimesoyl chloride concentration results in thicker membranes with a reduced specific surface area and consequently decreased water permeance. On the other hand, increasing the m-phenylenediamine concentration will accelerate the reaction rate and reduce the final crosslinking degree. A deeper understanding of the mechanism of polyamide-membrane formation is unveiled in this work, which can aid in the design of high-performance polyamide membranes in the future.

Strategic small molecule engineering: Unleashing the full potential of Kevlar aramid membrane in organic solvent nanofiltration

Kevlar aramid fiber (KANF), renowned for its exceptional solvent resistance, holds immense potential in fabricating of solvent-resistant membranes. However, the well-ordered structure of its rigid polymeric chains, coupled with intense intermolecular forces, significantly impedes the transport of solvents. Here, we propose a methodology utilizing small molecule polyethylene glycol (PEG) to mediate an interlayer structural reconstruction of KANF membranes, thereby enhancing solvent permeation. PEG, functioning as a nanostructure regulator, effectively inhibits the diffusion of DMSO into non-solvents during the phase inversion process. This intervention results in the multi-directional polymerization of aramid nanofibers and the emergence of distinctive interconnected microporous structures between layers, which notably accelerates the transport speed of solvents within the membrane. Concurrently, preserving of the dense layer on the surface ensures superior separation performance for the KANF membranes. This research underscores the possibility of modulating the internal microstructure of KANF membranes and highlights the prospective utility of KANF-PEG membranes in the organic solvent nanofiltration field.

Ultrafast Interfacial Self-Assembly toward Bioderived Polyester COF Membranes with Microstructure Optimization.

The precise manipulation of the microstructure (pore size, free volume distribution, and connectivity of the free-volume elements), thickness, and mechanical characteristics of membranes holds paramount significance in facilitating the effective utilization of self-standing membranes. In this contribution, the synthesis of two innovative ester-linked covalent-organic framework (COF) membranes is first reported, which are generated through the selection of plant-derived ellagic acid and quercetin phenolic monomers in conjunction with terephthaloyl chloride as a building block. The optimization of the microstructure of these two COF membranes is systematically achieved through the application of three different interfacial electric field systems: electric neutrality, positive electricity, and negative electricity. It is observed that the positively charged system facilitates a record increase in the rate of membrane formation, resulting in a denser membrane with a uniform pore size and enhanced flexibility. In addition, a correlation is identified wherein an increase in the alkyl chain length of the surfactants leads to a more uniform pore size and a decrease in the molecular weight cutoff of the COF membrane. The resulting COF membrane exhibits an unprecedented combination of high water permeance, superior sieving capability, robust mechanical strength, chemical robustness for promising membrane-based separation science and technology.

Fabrication of PVDF membranes via γ-ray irradiation and investigation into their membrane formation mechanisms and water treatment properties

Polyvinylidene fluoride (PVDF) membrane is a cheap and commonly used separation material, but its inherent hydrophobicity results in significant membrane contamination, which limits its engineering application and further development. The hydrophilic PVDF-g/co-NVP membrane was prepared through low-dose γ-ray irradiation and using N-vinyl-2-pyrrolidinone (NVP) as a modifier in this study. The effects of γ-ray dose and incorporating NVP additive on the microstructure, hydrophilicity, anti-fouling capability, and mechanical capacity of membranes were discussed. Molecular dynamics (MD) simulation method was used to comprehensively investigate the impact of the NVP on the physicochemical characteristics of membrane structure. Under a specific NVP load, the water contact angle of the membrane decreases from 87.92° to 52.66°. The pure water permeance reaches 362.1 L/m2 h, and the porosity increases to 55.21 %±1.29 %, which indicates that γ-ray irradiation with NVP addition can effectively adjust the pore structure and hydrophilicity of the membrane. During anti-fouling test against bovine serum albumin (BSA), the modified membrane exhibits remarkable anti-fouling characteristics, including reduced BSA accumulation, enhanced flux recovery, lower irreversible contamination level, and extended cleaning cycle compared with the original pure PVDF membrane because of its higher hydrophilicity and positive zeta-potential value. This study elucidates the mechanism underlying γ-ray graft modification of PVDF membranes, thereby providing valuable insights into the development of efficient functional membrane materials.

Ultrathin and Self-Supporting MOF/COF-Based Composite Membranes for Hydrogen Separation and Purification from Coke Oven Gas.

Coke oven gas (COG) is considered to be one of the most likely raw materials for large-scale H2 production in the near or medium term, with membrane separation technologies standing out from traditional technologies due to their less energy-intensive structures as well as simple operation and occupation. Based on the "MOF-in/on-COF" pore modification strategy, the COF membrane (named the PBD membrane) and ZIF-67 were used as assembly elements to design advanced molecular sieving membranes for hydrogen separation. The composition and microstructure of membranes before and after ZIF-67 loading as well as ZIF-67-in-PBD membranes under different preparation conditions (metal ion concentration, metal-ligand ratio, and reaction time) were investigated by various characterizations to reveal the synthesis regularity and microstructure regulation. Furthermore, H2/CH4 separation performances and separation mechanisms were also analyzed and compared. Finally, a dense, continuous, ultrathin, and self-supporting ZIF-67-in-PBD membrane with a Co2+ concentration of 0.02 mol/L, a metal-ligand ratio of 1:4, and a reaction time of 6 h exhibited the largest specific surface area, micropore proportion, and the best H2/CH4 separation selectivity (α = 33.48), which was significantly higher than the Robeson upper limit and was in a leading position among reported MOF membranes. The separation mechanism was mainly size screening, and adsorption selectivity also contributed a little.

Characterization of the microstructure, interfacial properties and crystallization behaviours of milk fat globule and membrane isolated from acidified bovine milk and sweet whey

Milk fat globule and membrane (MFGs/MFGM) ingredients are the main source of the phospholipid supplementation in the dairy industry. Their physicochemical properties and functionalities play important roles in their application. This study investigated the effect of acidification (pH 6.30 and pH 5.30) on the microstructure, interfacial and thermal properties of MFGs/MFGM sourced from bovine milk (control pH 6.70). Meanwhile, sweet whey was prepared to mimic the raw material used in the industrial production of MFGs/MFGM (MFGM-C). The study revealed a broad particle size distribution of MFGs/MFGM at pH 5.30, while smaller particles were found in MFGM-C. This was confirmed by confocal scanning microscopy (CLSM) images, which showed that few intact MFGs existed in the MFGM-C. Fourier Transform Infrared Spectroscopy (FTIR) indicated more peaks belonging to protein-lipids associations presented at pH 6.30. Additionally, the interfacial tension of MFGs/MFGM at pH 6.30 was significantly lower than at pH 6.70 and 5.30. X-ray Diffraction Spectra (XRD) showed that the fat in MFGM-C exhibited no detectable crystalline structures, and fewer α and β′ crystals appeared at pH 6.30. All MFGs/MFGM from bovine milk or whey exhibited both exothermic and endothermal events. The smallest heat enthalpy of crystallization (ΔHC) and melting (ΔHM) was observed in MFGM-C, followed by those at pH 6.30. Compared to MFGs/MFGM at pH 6.70, pH 6.30 induced more profound effects on the interfacial and thermal properties of MFGs/MFGM than pH 5.30. Acidification and the use of different raw materials lead to differentiation in the physicochemical and techno-functionalities of MFGs/MFGM.