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Wei, M.; Zhang, Y.; Wang, Y.; Liu, X.; Li, X.; Zheng, X. Application of Atomic Force Microscopy in Membrane Fouling. Encyclopedia. Available online: https://encyclopedia.pub/entry/54557 (accessed on 20 June 2024).
Wei M, Zhang Y, Wang Y, Liu X, Li X, Zheng X. Application of Atomic Force Microscopy in Membrane Fouling. Encyclopedia. Available at: https://encyclopedia.pub/entry/54557. Accessed June 20, 2024.
Wei, Mohan, Yaozhong Zhang, Yifan Wang, Xiaoping Liu, Xiaoliang Li, Xing Zheng. "Application of Atomic Force Microscopy in Membrane Fouling" Encyclopedia, https://encyclopedia.pub/entry/54557 (accessed June 20, 2024).
Wei, M., Zhang, Y., Wang, Y., Liu, X., Li, X., & Zheng, X. (2024, January 31). Application of Atomic Force Microscopy in Membrane Fouling. In Encyclopedia. https://encyclopedia.pub/entry/54557
Wei, Mohan, et al. "Application of Atomic Force Microscopy in Membrane Fouling." Encyclopedia. Web. 31 January, 2024.
Application of Atomic Force Microscopy in Membrane Fouling
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Membrane separation technology has emerged as the preferred method for producing clean water during wastewater treatment and desalination. This preference is attributed to the high separation accuracy, energy efficiency, lack of secondary pollution, and ease of operation of the technology. Membrane fouling is a key obstacle in membrane applications, including ultrafiltration (UF), microfiltration (MF), nanofiltration (NF), and reverse osmosis (RO). Membrane fouling is a particularly serious problem in the pre-treatment processes of industrial wastewater, leading to poor water quality and increased operating costs. A thorough understanding of fouling formation and properties is required in wastewater treatment using membranes and contributes to slowing down membrane fouling and implementing appropriate control measures. In response, extensive foundational investigations of membrane fouling have been conducted, with researchers seeking to clarify primary foulants, membrane–foulant interactions, and potential fouling mitigation techniques.

membrane fouling morphology roughness interactions

1. Characterization of Membrane

The interaction between the membranes and foulants is related to the membrane surface properties, such as hydrophilicity, roughness, and charge. The development of high-quality antifouling membranes could reduce the interaction forces between foulants and membrane surfaces and decelerate membrane fouling. The technique facilitates the visualization of membrane surfaces at high resolution, characterizing three-dimensional presentation of membrane surface information, allowing for an exhaustive detailed expression of the surface characteristics of the membrane. 

1.1. Characterization of Membrane Morphology

Visualization of the membrane surface morphology aids in understanding the relevant properties of the membrane. Atomic force microscopy (AFM) excels in visualizing morphological features, allowing for the in situ characterization of morphological changes occurring at the interface of functional layers on membrane surfaces during the polymerization process. During the phase inversion process, utilizing AFM to scan nanofiltration or reverse osmosis membranes prepared under various parameters in a liquid environment enables the in situ observation of more detailed and systematic changes in the surface functional layers [1]. Further, AFM can be used to investigate the degradation effects of soil microbial communities on polyethylene membranes by observing changes in the microstructure of the membrane [2]. Using AFM, it is also possible to observe the ion transport channels of membranes. Examination of modified anion exchange membrane (AEM) materials with densely grafted ionic clusters through atomic force microscopy can reveal distinct ion conduction pathways and demonstrate that the modified AEMs exhibit excellent nano-phase separation [3]. By studying the surfaces of nanofiltration membranes using AFM in different imaging modes, various AFM imaging mode characteristics can be obtained [4]. The tapping mode in AFM allows for precise measurement of the 3D structure of soft and delicate surfaces without damaging their morphology. This technique is particularly useful for studying the interfacial polymerization process of active functional layers on nanofiltration membrane surfaces [5].
Evidently, AFM can be used to understand membrane layer surface smoothness and uniformity; capture membrane surface microscopic morphology, including surface defects, nanoscale protrusions, or depressions; and provide intuitive images of membrane surface morphology. Thus, AFM is not only capable of in situ measurement of surface morphology changes induced by hydrochemical conditions, but also enables the understanding and discovery of ion transport channels and nanoscale morphologies through 3D visualization images. Particularly, the tapping mode is almost non-destructive to thin and soft membrane surfaces. Additionally, AFM can be used to study the surface potential signals of membrane materials, overlaying them with the physicochemical properties of specific areas. These aspects are crucial for characterizing membrane performance and understanding membrane fabrication.

1.2. Characterization of Roughness

The surface roughness of a membrane is a key factor influencing interfacial performance and fouling processes. Using AFM not only allows for the observation of a membrane’s surface morphology, but due to its three-dimensional measuring capabilities along the x, y, and z axes, AFM can also precisely characterize in situ the roughness of the membrane surface/functional layer and provide detailed 3D surface topography maps. AFM can be used to understand the roughness of various types of membranes, such as cation exchange membranes. During long-term operation, AFM can precisely measure changes in roughness, thereby establishing the relationship between roughness and ion exchange performance. This enhances the monitoring of the ion exchange effectiveness and contamination level of cation exchange membranes [6].
In the process of membrane modification, the incorporation of specific active components, such as surfactants or polymer monomers, in the adsorption crosslinking process can increase surface roughness and alter the structure of the membrane’s functional layer. Similarly, modifications with carbon nanotubes, metal oxides, and other substances can change the membrane’s morphology, increase roughness, and expand membrane channels, thereby altering the membrane’s performance. Using AFM, changes in membrane surfaces and channels can be observed, and the roughness can be accurately measured. Roughness serves as an important parameter in membrane fabrication. The results generally show that the surface of the original membrane is low in roughness, uniform, and smooth. When modifiers or carbon nanotubes are added, nanoscale modified structures are formed, increasing the roughness. This enhancement in roughness can improve the membrane’s anti-fouling properties, permeation evaporation performance, ion selectivity, and regulate the membrane’s hydrophilicity or hydrophobicity. Asymmetric polystyrene membranes manufactured using the wet phase inversion method with the addition of surfactant (Pluronic F127) increase the surface roughness of the membrane and strengthen the membrane channels, significantly enhancing the permeation evaporation performance of the membrane [7]. Similarly, analysis of multi-walled carbon nanotube (MWCNT) dispersed PS nanofiltration membranes [8] using AFM shows that the surface of the original PS membrane is smooth and uniform, while the addition of MWCNTs increases the surface roughness and makes the structure more evident, thus improving the hydrogen permeability of the PS membrane. Roughness measurements using AFM reveal that plasma treatment and surface acidification also increase the roughness of ion exchange membranes, enabling more ion exchange and facilitating the preparation of ion exchange membranes with excellent performance [9].
However, studies show that for rough surfaces, nanoscale modified structures have better tendencies to prevent membrane fouling, but when the modified structures are too large, they can exacerbate membrane fouling. These related insights can be obtained through the precise measurement of roughness using AFM. In addition, modifying the membrane surface through copolymerization and grafting methods can increase membrane roughness, and AFM can measure roughness changes during the membrane modification process in situ. When characterizing hydrophilic polymer-functionalized polysulfone (PSF) blend membranes using AFM [10], researchers found that the addition of 4VP side chains enhanced the surface roughness of the modified membrane. In another study, PSF membranes modified with titanium oxide compounds [11] had higher surface roughness, and these modified membranes exhibited excellent hydrophilicity and anti-fouling properties. Simple coding of the surfactants polydopamine and 3-(N, N-dimethyl myristoyl) propane sulfonate [12] can achieve anti-fouling properties of polyethersulfone (PES) ultrafiltration membranes. Scanning these modified membranes with AFM can obtain roughness parameters Rq and Ra, indicating that the modified membranes significantly mitigate flux decline and enhance anti-fouling performance.
Precise measurement of membrane surface roughness with AFM can be used to explore which roughness is more resistant to contamination on the modified membrane surface, thus achieving membrane performance adjustment. Although many studies have shown that increased roughness may lead to increased tendencies for membrane fouling [6][10], other research findings suggest that adding micrometer to nanometer-sized particles to increase surface roughness (similar to lotus leaf biomimetic structures) can reduce membrane fouling [8][9]. This discrepancy is mainly because a single roughness parameter is insufficient to summarize the complexity of membrane surface fouling. Establishing a relationship between roughness R measured with AFM and the roughness index H can more quickly and accurately evaluate membrane surface roughness [13]. In addition, an overall assessment should combine AFM with various other techniques to carefully examine membrane surface characteristics, such as surface potential, hydrophilicity/hydrophobicity, functional groups, and foulant properties. Through this comprehensive judgment of characterization results, the relationship between surface roughness and membrane fouling can be thoroughly analyzed. Establishing the relationship between membrane surface roughness measured by AFM and membrane surface potential, functional groups, etc., can better help optimize membrane hydrophilicity/hydrophobicity, permeation selectivity, ion selectivity, and anti-fouling properties, providing guidance for the design and optimization of membrane interfaces.

1.3. Measurement of Membrane Channels

Membrane channels are crucial for the filtration performance of membranes, as the size and structure of these channels directly influence the membrane’s selectivity and permeation flux, which relates to the trade-off effect of the membrane. AFM has been utilized to detect various surface parameters of modified membranes, including the structure and pore size of membrane channels. These researchers [14][15][16][17][18][19] characterized the surfaces of modified membranes using AFM and found that the deposition process of modifiers made the membrane surfaces smoother, eliminating small-scale rough features, reducing pore sizes, and decreasing sensitivity to foulants. For instance, Kim et al. [15] achieved atomic-level surface functionalization of nanofiltration membranes using graphene oxide (GO) combined with plasma-enhanced atomic layer deposition (ALD) technology. A novel data analysis method [14] integrating AFM with “pore reconstruction technology” was used to assess membrane channel structures, including size, shape, and interlayer distances. The obtained membrane channel information is vital for the permeation selection process in membrane desalination and can also serve as a crucial factor in assessing the propensity for membrane fouling. AFM can precisely measure the interlayer distances of zinc oxide-coated aluminum membrane channels modified by deposition methods [16], identify the membrane channel structures of superhydrophilic copper mesh membranes coated with zinc oxide nanostructures (ZnO NW) used for oil–water separation [17], acquire information about the shape of membrane channels in modified seawater desalination nanofiltration membranes created using molecular layer deposition (MLD) techniques [18], and obtain 3D shape information of membrane channels in chitosan and polystyrene sulfonate-modified polyamide microfiltration membranes prepared by layer-by-layer (LBL) deposition methods [19].
Combining the surface and cross-sectional images obtained from AFM can construct three-dimensional images of membrane channels, providing detailed information on the size, shape, and arrangement of channels, and more accurately predicting the degree of membrane channel clogging and membrane fouling. Studies indicate that uniformly distributed pore structures, as opposed to uneven distributions, are likely to reduce the risk of fouling. The systematic distribution of pores in uniform membranes can enhance the interception capacity for foulants [20]. Notably, the geometric shape of membrane channels greatly influences membrane fouling. Typically, the fouling intensity caused by slit-shaped pores is lower than that caused by circular pores [21]. Additionally, AFM can accurately present the degree of membrane channel clogging and the state of membrane fouling in real liquid-phase environments. In contrast, SEM requires measurements under dry and vacuum conditions, which may lead to distorted results and inaccurate pore information. Therefore, membrane channel data obtained through AFM are crucial for tracking membrane fouling trajectories and assessing and improving membrane performance.
As previously mentioned, employing AFM to characterize different membranes allows for a more comprehensive observation of three-dimensional surface morphology, membrane roughness measurements, membrane channel assessments, and an overall evaluation of the material characteristics and application performance of membranes and modified membranes. As depicted in Figure 1, this section categorizes and summarizes the different modes, characteristics, and outcomes of modified membrane characterization via AFM as referenced in the mentioned literature. AFM has also been extensively applied in characterizing modified membranes of various materials, such as modified Langmuir–Blodgett (LB) thin films [22], uniquely shaped modified block copolymer microfiltration membranes [23], zeolite-filled polyethersulfone membranes [24], modified Carbosep M5 ceramic membranes [25], innovative positively charged nanofiltration membranes [26], organic membranes for oil–water separation [27], and composite ceramic microfiltration membranes for greywater treatment [28]. This technique (atomic force microscopy) has become a powerful tool in the design and fabrication of functional membranes.
Figure 1. Different aspects and results of AFM characterization of modified membranes in different modes.

2. Characterization of Contaminants

Different types of membrane foulants are encountered in membrane-based technologies and in other techniques; therefore, employing AFM for scrutinizing the characteristics of contaminants at a microscopic level is vital. The nanometer-scale resolution of AFM enables direct observation of the contaminant morphology and structure on membrane surfaces. Accordingly, AFM could be used to monitor the adsorption and adhesion of contaminants in real-time under various environmental conditions. Morphological changes in living microorganisms during metabolism could be recorded in tapping or non-contact modes, which is a challenge for other techniques. Employing the capabilities of AFM in this way enhances understanding of membrane fouling mechanisms. Characterizing contaminants facilitates superior understanding of membrane fouling principles, and offers essential guidance for the design, operation, and maintenance of membrane filtration systems. This is an important factor in the investigation of membrane fouling mechanisms.

2.1. Organic Contaminants

Natural organic matter (NOM) is the primary contaminant in wastewater. It is a complex heterogeneous system comprising diverse organic molecules [29], such as humic substances, polysaccharides, and proteins, which can all affect the membrane performance. Observations using AFM in aquatic environments have revealed that natural polysaccharide sodium alginate (SA) predominantly exists as single helical chains, with diameters of approximately 0.2–0.3 nm [30]. Scanning humic acid sodium (HA)-contaminated mica surfaces with AFM has uncovered spherical particles and aggregates, featuring colloidal diameters under 100 nm and heights from 0.5 to 7 nm [31]. In studies on protein membrane fouling, most protein molecules have been observed as monomers on mica surfaces [32]. Extracellular organic matter (EOM) can lead to severe ultrafiltration membrane fouling. AFM enables the observation of the aggregation and blockage behaviors of pollutants on the membrane surface [33], and evaluates the effects of cleaning/pre-treatment [34]. Utilizing AFM technology aids in further understanding the impact of natural organic matter (NOM) on membrane performance during water treatment processes, thereby laying the foundation for mitigating organic membrane fouling.

2.2. Biological Contaminants

In addition to typical organic contaminants, biological contaminants can impair membrane treatment efficiency in water treatment processes. Escherichia coli is a common pathogenic microorganism that compromises the safety of water resources and drinking water. Researchers have used AFM to investigate the morphological changes in E. coli on membrane surfaces under varying pH conditions [35] and correlate it with membrane filtration and cleaning [36]. In addition, AFM has been used to examine changes in the morphology of antibiotic-resistant E. coli on membrane surfaces during photocatalytic Fenton water treatment [37]. Recently, owing to the potential problem of microalgae in water treatment processes, particularly in membrane treatment, AFM has been applied extensively to study microalgal cell morphology and nanomechanical properties on membrane surfaces. High-speed atomic force microscopy (HS-AFM) has been employed to analyze Chlorella vulgaris treated with electrocoagulation flotation (ECF) [38]. Another study used AFM to determine the energy required to disrupt individual microalgae cells [39]. Guidance could be offered for alleviating biological fouling caused by microalgae. For the living microbial cells, AFM-based single-cell force spectroscopy (AFM-SCFS) has significant value for characterizing the structure, mechanical properties, and molecular activity of individual living microbial cells [40]. The technique can measure the mechanical properties of a single microorganism, quantify individual microorganism adhesion forces, and perform structural imaging of microbial behavior while simultaneously sensing microbial activity in real-time. Wang et al. [41] employed AFM to explore the dynamic effects of various environmental factors on microorganisms and membrane surface interactions at a molecular scale. This provides a research basis for the effective inhibition of biological foulants on membrane surfaces.
AFM-SFCS allows sensitive measurements of the mechanical properties of individual molecules. This allows researchers to gain insight into the mechanical properties of individual molecules such as stretching, deformation, and fracture, which is important for understanding the properties of biomolecules, polymers, and other materials. Nevertheless, AFM-SCFS has not reached maturity yet and still presents several technical challenges. Based on the group’s research on AFM-SFCS in the environmental field, researchers found that this technology faces the following problems in its application. First, the adhesion of live single cells to the probe tip is difficult and requires the selection of suitable adhesives for cell immobilization. Additionally, assessing the viability of single cells on the probe tip after attachment is challenging, prompting researchers to explore more advanced methods for examining post-adhesion cell viability. The morphology of single cells is not consistent; it encompasses rod or spherical shapes and other irregular shapes. During the adhesion process, it is crucial to consider different adhesion positions and variations in contact areas with the measurement surface to prevent inconsistencies in the recorded force magnitudes. Furthermore, even when live cells successfully adhere, it is difficult to maintain consistent single-cell activity at the probe tip (considering the different activity levels of young and aged cells at various stages). Ongoing investigation and refinement of AFM-SCFS techniques is anticipated to address these issues in the near future. Researchers could, therefore, gain better understanding of the characteristics of biological contaminants using AFM technology, further elucidate the membrane fouling process, guide biofouling removal, and offer theoretical support and practical guidance for the development of long-lasting antifouling membrane materials and superior biofouling control strategies.

2.3. Emerging Contaminants

Emerging contaminants in wastewater treatment processes, such as microplastics, antibiotics, and endocrine-disrupting compounds (EDCs) have been attracting increasing academic attention at national and international levels. As a high-resolution tool, AFM enables a more detailed examination of the physical properties of microplastics [42]. For instance, Melo-Agustín et al. [43] employed AFM for morphological analysis of microplastic surfaces, discovering that polyethylene (PE) microplastic surfaces exhibit higher levels of roughness than polypropylene (PP) microplastic surfaces. This observation suggests that PE is more susceptible to degradation than PP, potentially leading to greater contaminant adsorption. Chen et al. [44] introduced a method that combines AFM with infrared spectroscopy (AFM-IR) to characterize nanoplastics (NPs). This hybrid AFM technique can identify and image the chemical composition of nanoplastics at a high spatial resolution (20–100 nm), thereby offering a novel approach to NP characterization. However, the large specific surface area of microplastics often causes them to function as ‘carriers’ of other contaminants during water treatment processes, which exacerbates pollution. For instance, Zhang et al. [45] employed AFM to determine the interaction forces between NPs (hematite and corundum) and Escherichia coli cells, gaining further understanding of the membrane fouling mechanism of microplastics.
Additionally, antibiotics are frequently occurring emerging pollutants in aquatic environments, and even at trace concentrations, antibiotics in wastewater can adversely affect human health. AFM can effectively characterize the morphology and interaction forces of antibiotics on the membrane surface, thereby enhancing the efficiency of membranes in intercepting them. For instance, Liu et al. [46] used AFM to investigate the adsorption of EDCs on nanofiltration membrane surfaces, subsequently enhancing the EDC removal rate by preparing modified nanofiltration membranes. Wu et al. [47] attached sulfamethoxazole (SMX), a representative antibiotic, to an AFM tip to measure the SMX adhesion force distribution. Their study revealed the adhesion mechanism of SMX and, potentially, that of other sulfonamide antibiotics at a molecular level from both experimental and theoretical viewpoints. Researchers have also examined the impact of microplastics on antibiotic transport during sand filtration [48] by grafting ciprofloxacin (CIP) and sulfamethoxazole (SMX) onto AFM probes to determine the adhesion forces between representative microplastics (PS and PE) and quartz sand. Their study explored the mechanism of microplastics that enhances antibiotic transport in sand filtration systems from the perspective of molecular interactions. Table 1 summarizes the entire literature on different aspects of AFM studies of different pollutants in this section. In summary, employing AFM to investigate contaminant morphology under various water treatment conditions contributes to a deeper understanding of the characteristics of the contaminants, which, in turn, could inform the removal of attendant membrane foulants.

3. Microscopic Identification of Membrane Fouling Processes under Changing Factors

The previous text, respectively, introduced the membrane and contaminants observed by AFM. However, membrane fouling is a complex fouling process influenced by multiple factors. Therefore, the research team conducted abundant research on the effects of changes in the ionic concentration, pH, and time on membrane fouling using AFM. By employing AFM, researchers can monitor the morphological changes in contaminants under various environmental conditions, facilitating real-time observation of the adsorption process on membrane surfaces. Once contaminants are adsorbed, alterations in environmental factors (ionic conditions, pH, membrane surface properties, and time) could cause varying fouling morphologies and characteristics compared with their initial states. 
Ionic conditions: the research team [49][50][51][52] used AFM to study the effects of different valence ions on membrane fouling of NOMs. Using AFM force measurements, morphology characterization, and other technical methods, the effect of monovalent ions such as Na+ and K+ on organic compounds was found to be based on their charge and structure. However, the effect of divalent ions such as Ca2+ and Mg2+ on organic compounds also included complexation. Among them, it is closely related to the special functional groups, types, and structures of NOMs. Miao et al. [55][56] employed AFM to investigate the effects of Na+, Mg2+, and Ca2+ on HA fouling through HA membrane fouling experiments. These authors observed that membrane fouling intensified at lower Ca2+ or Mg2+ concentrations and significantly decreased at substantially higher Ca2+ or Mg2+ concentrations, albeit with the two ions having different mechanisms.
pH: Researchers investigated changes in membrane fouling under different pH conditions using AFM [51]. The results showed that at a pH range of 4–6, the adherence of polysaccharide fouling, and its reversibility, depended on the functional groups. When the organics were rich in –COOH, an increase in pH reduced their deposition on the membrane surface and alleviated adsorptive fouling and irreversibility. For the –NH2 functional group, an increase in pH led to more severe polysaccharide fouling owing to a lower degree of protonation, and the resulting fouling was highly irreversible. Modification using GO alleviated the adsorptive fouling of these two polysaccharides on PVDF; however, the extent of alleviation depended on the abundance of functional groups on the polysaccharides.
Time: Interestingly, researchers found that time changes could affect membrane fouling [41]. Researchers studied the pollution behavior of three selected model foulants at different adsorption times. For the SA-Ca2+ system, a longer adsorption time slightly increased the adsorption capacity of SA but significantly reduced its reversibility. With regards to BSA-Ca2+, the extended time did not change the amount of BSA deposited on the membrane surface but led to more residual BSA after cleaning. Similarly, in the HA-Ca2+ system, the adsorption time had almost no effect on the adsorption amount of HA but reduced its reversibility. Duration had a significant effect on the quantity and reversibility of membrane fouling, depending on the chemical properties of the membrane. Therefore, the AFM measurement results indicate that the longer the adsorption time, the denser the fouling layer and the stronger the interaction force between the fouling membranes.
Other factors: Researchers also used AFM to study the effects of voltage on the fouling of a novel polypyrrole (PPy) and stainless steel mesh conductive composite membrane [54]. Researchers found that the PPy ‘cauliflower’ structure expanded as the applied voltage increased, and the corresponding roughness of the feature area gradually decreased from 5.91 to 4.34 nm. This result could probably be ascribed to the delocalized conjugated electron carrier in the conducting polymer moving along the polymer chain under an external electric field, which changed the dipole moment of the PPy molecules. Such change caused changes in the conformation and intermolecular arrangement of the PPy molecules, resulting in the expansion of surface morphology and, thereby, decreasing the roughness.
In addition to the these membrane fouling investigations, Arkhangelsky et al. [57] employed AFM to investigate the membrane-cleaning process and examined the influence of different cleaning agents on membrane surfaces. Analysis employing AFM revealed that the sodium hypochlorite (NaOCl) cleaning agent affected the contaminants and the membrane, leading to partial organic matter destruction and a modified membrane surface. In contrast, sodium hydroxide (NaOH) treatment completely destroyed the proteins, yielding a smooth surface with minimal residual matter. Similarly, using AFM to examine the fouling behavior of BSA on the membrane, it was found that pre-chlorination significantly mitigated membrane fouling, whereas pre-ozonation oxidation exacerbated it [53]. These studies leveraged AFM technology to characterize the morphology of common contaminants on membrane surfaces and to elucidate the alterations and characteristics of the membrane fouling surface morphology under various conditions, such as time and pH. This information provides a theoretical basis for the mechanism of converting irreversible fouling into reversible fouling, and effectively informs membrane fouling control strategies.

4. Measurement of Interactions in Membrane Fouling

In the membrane treatment process, the micro-interaction between membranes and foulants significantly affects the formation of membrane fouling. The AFM technology offers valuable insights into the characteristics of foulants and membrane–foulant interactions, which could be leveraged to develop more effective strategies for preventing and controlling membrane fouling. Such strategies include optimizing membrane materials and surface modifications, enhancing pre-treatment processes, and creating innovative cleaning and regeneration technologies, which could reduce operational costs and prolong the lifespan of the membranes. The interaction force between foulants and the membrane is crucial for determining the efficiency of membrane fouling removal. Nanomechanical measurements using AFM and the quantification of interfacial interaction forces during membrane fouling provide essential information on the nanomechanical properties of foulants and membrane surfaces. Such information is critical for understanding membrane fouling.
The type of AFM colloidal probe fabricated plays a key role for the interaction force measurements. Combining AFM with BSA-adsorbed SiO2 microsphere colloidal probes to investigate membrane surface fouling in the presence of BSA [58]. These authors observed that the adhesion force between PVDF-BSA were −1.5 nN, whereas the adhesion force between BSA-BSA were nearly zero, suggesting that BSA fouling behavior was predominantly influenced by the physicochemical interaction between the membrane polymer and BSA. Membrane-coated colloidal probes made of SiO2 microspheres coated with PP/PA are utilized in AFM to investigate the mechanism of membrane fouling caused by HA [59]. Force measurements showed that the interaction between the membrane and foulants was the primary factor contributing to the membrane fouling behavior. In a study of membrane fouling involving HA and SA [60], indention and retraction curves obtained from force spectroscopy measurements using an AFM probe modified with silicon nitride were used to characterize the surface stiffness and adhesive properties of fouled and clean membranes. These authors discovered that bacterial cells neither adhered to nor penetrated the organic fouling layer but, instead, traversed the thin foulant layer and directly adhered to the membrane surface.
To further understand and clarify the fouling behavior of HA and SA on membranes, Miao et al. [61] used AFM in conjunction with PVDF and foulant-coated probes to investigate the intermolecular forces between the membrane and contaminants (SA, HA, or HA/SA mixtures), as well as the forces between the contaminants themselves. Owing to the strong interaction between the hydroxyl groups in SA and PVDF, the adhesion force between PVDF and SA was more than double that of PVDF-HA. The formation of organic fouling on membranes can be studied by adsorbing the corresponding EfOM components onto the surface of PVDF microspheres sintered on cantilevers prepared to form EfOM-coated colloidal probes [62]. Using AFM, these authors demonstrated that the adhesion force between PVDF and different parts of the EfOM follow the order PVDF-TPI (affinitive) < PVDF-HPO (hydrophobic) < PVDF-HPI (hydrophilic). Several researchers have examined membrane fouling under the combined action of BSA and HA [63]. They created colloidal probes with BSA directly attached to the probe tip and employed AFM-based chemical force spectroscopy for adhesion force measurements. Furthermore, employing AFM to examine the interaction energy between polyvinyl chloride (PVC) membranes and three water contaminants, namely HA, BSA, and dextran (DEX) [64], helps in revealing the complex mechanisms of related membrane fouling.
Analyzing the AFM results for the interaction forces between individual and multiple organic contaminants with membranes has led to the following conclusions. Generally, the interaction between membranes and foulants is stronger than the interaction forces among the foulants themselves. HA adsorption significantly decreases the BSA adhesion force on hydrophobic surfaces. The fouling rate of PVC membranes follows the order of DEX > BSA > HA, demonstrating that selecting suitable pretreatment processes to remove specific foulants can effectively control polyvinyl chloride membrane fouling. Owing to the strong interaction between the hydroxyl groups in SA and PVDF, SA, rather than HA, has been identified as the primary cause of PVDF membrane fouling. This implies that the pretreatment process for removing SA is crucial in controlling PVDF membrane fouling. It suggests that employing appropriate methods, such as pretreatment, membrane modification, or cleaning, to reduce the hydrogen bonding interactions between PVDF and foulants is an effective strategy for reducing adhesion forces. Choosing pretreatments that convert HPI and HPO fractions into TPI fractions is essential for controlling PVDF membrane fouling during secondary effluent filtration. Therefore, AFM force measurements provide valuable information for selecting membrane modifications, feedwater pretreatment, and cleaning technologies in wastewater treatment and desalination.
Recently, AFM has increasingly been employed to investigate the interaction forces between various foulants and membranes. Single force spectroscopy curves from AFM are used to assess the interactions between membranes and foulants, serving as a crucial parameter for adjusting the properties of modified membranes. This technique can measure not only the interaction forces between hard objects but also those involving softer entities, such as in the interaction force measurements between pretreated modified membranes and related membrane foulants [65]. Scholars have used AFM’s single force spectroscopy curves to elucidate the mechanism of scaling in electrodialysis induced by anionic polyacrylamide (APAM) in anion exchange membranes (AEM) [66]. AFM can also characterize the interaction forces between various coatings and other substances, apart from membranes, such as the interactions between bubbles in different solutions [67], dissolved organics [68], and spherical particles of asphalt coating. It can also measure the interactions between living microorganisms and membranes, which is vital since living cells, being alive, secrete exosomes under external forces and their interaction forces with membranes change under stress conditions. Using AFM to measure these forces can more accurately reflect the biological fouling on membrane surfaces. Yumiyama and others [69] directly measured the interaction forces between individual yeast cells. Scholars have also studied the adhesion forces between yeast cells and microbubbles (MB) [70]. These studies demonstrate the utility of AFM’s single force spectroscopy curves in measuring the interaction forces between foulants and membranes, which can be used to evaluate the characteristics and interactions at the membrane–foulant interface. This aids in developing high-performance modified membranes and more effective membrane cleaning methods.

5. Modeling or Analysis of the Interaction in Membrane Fouling

In understanding membrane fouling processes, the characteristics of impurities (such as size, shape, charge properties, and chemical stability) and the attributes of membrane materials (such as pore size, surface roughness, chemical stability, and charge properties) significantly influence the interaction modes between impurities and the membrane. Certain impurities could interact more strongly with specific membrane materials, potentially leading to severe membrane fouling. For example, positively charged impurities could be strongly adsorbed onto negatively charged membrane materials, forming a fouling layer. Conversely, if repulsive forces are generated between the membrane material and the impurities because of their charges, the degree of fouling could decrease. Ionic composition can also have a significant impact on foulant–foulant interactions [71]. Therefore, the modeling and analysis of such interactions could provide key insights for predicting and optimizing the performance of membrane processes.
By combining the results of AFM force measurements with certain existing theories or models, such as the extended Derjaguin–Landau–Verwey–Overbeek (XDLVO) theory [72][73] and the Hermia model [74][75], it is possible to predict the manner in which forces act as particles approach the membrane surface, as well as their impact on particle adsorption behavior. This allows for the prediction of membrane fouling based on molecular characteristics. Wang et al. [49] employed the XDLVO model to calculate the interaction energy between PVDF membranes and organic matter under different ionic strengths, finding that as the Na+ concentration increased, the Lewis acid–base (AB) force values gradually decreased. The AB forces are related to the chemical functional groups of the particles and the membrane [76]. This result shows that an increase in ionic strength enhances the AB interaction between the membrane and organic matter, which is consistent with the total amount of organic matter adsorbed on the membrane surface as the ionic strength increases. Not only that, XDLVO interactions and surface roughness may collectively influence the transport and fate of emerging multifunctional nanohybrids in the environment [77]. In addition, these authors [78][79] found that the results calculated by the XDLVO theory aligned with the AFM analysis results, suggesting that AFM force–distance curves could effectively validate the calculated results and that AFM is highly reliable for measuring the interactions between the membrane and foulants. Integrating AFM force measurement techniques to analyze blocking mechanisms during membrane filtration [74] aids in better understanding the phenomenon of membrane fouling and in developing effective fouling prevention strategies.
The Hermia model [75], by fitting the relationship between apparent fouling resistance and membrane filtration time, identifies the types of fouling caused by different blocking mechanisms [80]. Huang et al. [81] developed the Unified Membrane Fouling Index (UMFI) based on the Hermia model. By directly testing commercial membranes, UMFI can quantify the likelihood of membrane fouling, which is very useful for evaluating fouling observed in low-pressure membranes (LPMs) across different water treatment scales. AFM force measurement technology can be used to validate these established models, helping to deepen the understanding of membrane blocking mechanisms.
It should be noted that although the XDLVO theory and Hermia model provide useful insights, they do not encompass all types of fouling behavior. These theories and models are more suitable for predictions under steady conditions, whereas actual water treatment processes are conventionally confronted by more complex, dynamic, and changing conditions. New research seeks to integrate experimental and theoretical approaches for a more comprehensive understanding and prediction of the interactions between impurities and membrane materials. For example, AFM and other nanoscale characterization techniques are used for direct observation and measurement of the interactions between impurities and membranes, whereas molecular dynamics simulations and quantum chemical calculations are used to understand these processes at the atomic scale. Analyzing and modeling the potential interactions between different impurities and membrane materials is a key factor in membrane science and engineering. Integration of various experimental and theoretical methods is required to gain a comprehensive and in-depth understanding. In this process, AFM could predict the adsorption tendency of pollutants by measuring the interaction forces between the pollutants and the membrane surface. Further, AFM could also monitor the fouling process, such as adsorption, diffusion, and aggregation of pollutants on the membrane surface in real-time. Combining AFM with relevant theories and models helps to further the exploration of the membrane fouling process and the prediction of membrane fouling trends.

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