Emerging Materials and Technologies for Water and Wastewater TreatmentView this Special Issue
Fast and Versatile Pathway in Fabrication of Polyelectrolyte Multilayer Nanofiltration Membrane with Tunable Properties
Thin film composite nanofiltration (NF) membranes are relatively new membranes compared to other types of pressure-driven membranes. However, they attract interest from researchers due to their versatility to be used in various applications. In this work, a new class of NF membrane was successfully fabricated through spin-assisted layer-by-layer assembly by depositing alternate layers of branched polyethylenimine (PEI) and poly(sodium 4-styrenesulfonate) (PSS) on ultrafiltration polysulfone (PSF) membrane. The suitability of the fabricated membranes for removal of divalent ions was investigated. It was found that the membrane consisting of (PEI/PSS)10–0.05 M NaCl showed MgCl2 rejection rate of 93.95% and permeation flux of 0.9 L/m2·h bar during tests performed using a crossflow permeation cell at a crossflow velocity of 0.65 m/s, MgCl2 feed concentration of 6530 ppm, pressure of 10 bar, temperature of 32.5°C, and pH of 6.5. This result suggests that this new fabrication method is suitable for producing polyelectrolyte multilayered (PEM) NF membranes that exhibit comparable membrane performance to commercial ones.
Among pressure-driven membranes, a nanofiltration (NF) membrane is considered as the most recently developed one. The NF membrane is known for its ability to reject multivalent ions and organic compounds coupled with high permeation flux. Owing to these characteristics, the use of NF particularly in water treatment becomes more and more popular particularly in water treatment applications such as removal of multivalent ions [1, 2], heavy metals [3–5], pesticides [6, 7], dyes , and textiles .
As for other pressure-driven membranes, NF also suffers from fouling. Rapid fouling film formation causes significant flux decrease which can hurt the operation of this membrane especially in terms of operational cost. In severe cases, it even becomes necessary to replace the membrane. Membrane cleaning and replacement account for up to 6% and 16%, respectively, of the total water treatment costs . Thus, improving the fouling resistance of these membranes has become essential for reducing the above-described costs.
It is generally accepted that the physicochemical properties of membranes, such as their roughness, surface charge, foulant-membrane surface interactions, and hydrophobicity, are the primary factors affecting their fouling characteristics. The primary source of these problems is the membrane material itself. Several common commercial polymers such as poly(ether sulfone) (PES), polyamide (PA), and poly piperazine amide (PPA) are used extensively for NF/reverse osmosis (RO) membranes, making up 91% of the total sales . For instance, PA is used by GE-Osmonics to produce Desal 5 DL®, NF90®, and Desal 51HL®; meanwhile, PES is used by Nitto Denko to fabricate NTR7450®, whereas PPA is used by Toray and Film Tech to prepare UTC-20® and NF-400®, respectively.
All these membranes, and particularly polyamide membranes, are hydrophobic and exhibit relatively rough surfaces. As a result, these NF membranes are especially susceptible to fouling. Unfortunately, research on commercial Reverse Osmosis (RO)/NF membranes from a chemistry viewpoint has been stagnant for some time now, with there being no major developments in the last couple of decades [11, 12].
It is suggested that, with respect to fouling, both the membrane chemistry and the fabrication technique used play a significant part, as they have a determining effect on the physicochemical properties of the membrane in question. Thus, research efforts in the last two decades have primarily been directed toward the development of novel membrane materials, including inorganic ones, as well as those incorporating nanoparticles and polymers with high hydrophilicity and having smooth surfaces .
In order to tackle both fabrication technique and membrane chemistry all at once, it is imperative to try out several new emerging thin film fabrication techniques that truly provide access to control the properties of the film to nanoscale and also offer flexibility from chemistry point of view. Among thin film fabrication techniques, layer-by-layer (LbL) assembly is considered to be the most versatile and most robust technique .
In LbL assembly, ultrathin layers with thicknesses of the order of the subnanometer scale can be deposited alternately on a support layer. Hence, the final thickness of the active layer can be fine-tuned to the desired level merely by varying the number of deposition cycles. One can also easily change the membrane surface charge by terminating the assembly process at the deposition of a material with the desired charge (positive, negative, or neutral). For this purpose, typically polyelectrolyte is employed because they are typically hydrophilic and exhibit a charge either positive or negative. This technique itself can utilize various materials including organic, inorganic, or even microorganism.
Principally, there are three approaches for fabricating LbL-assembled films, namely, dipping, spraying, and spinning. Spin-assisted LbL (SA-LbL) assembly is believed to be the fastest method and also the most suitable one for producing membranes with the smoothest surfaces [14, 15]. There have been several works done for the use of conventional dip-LbL in NF application [16–25]; meanwhile, the use of SA-LbL assembly for fabrication of NF membrane is still at infancy. However, our previous works showed that SA-LbL can be successfully used to fabricate this membrane with outstanding properties [26–29].
Based on the above literature review, in this work, spin-assisted LbL (SA-LbL) assembly is utilized for fabricating NF membranes suitable for removing divalent salts such as MgCl2 from water. Also, as part of continuous work in finding the most suitable materials that provide high rejection, high flux, and less susceptible to biofouling, two other polyelectrolytes are used, namely, polystyrenesulfonate (PSS) and poly(ethylene imine) (PEI). Number of layers and pH assembly of polyelectrolyte were studied since PEI is weak polyelectrolyte whose degree of ionization is strongly affected by assembly and external pH.
2. Materials and Methods
In this work, branched-polyethylenimine (PEI) with molecular weight of 25,000 and poly(sodium 4-styrenesulfonate) (PSS) with a molecular weight of 70,000 in the form of a 30 wt% in H2O solution were purchased from Sigma-Aldrich (USA). Extra-pure NaCl was obtained from Scharlau (Spain) while extra-pure MgCl2•6H2O was obtained from Loba Chemie Pvt. Ltd. (India).
Stock solutions containing 0.02 M polyelectrolytes (PEI and PSS) containing additional NaCl concentration of 0.05 M were prepared. In these experiments, the pH of the PEI and PSS solution were varied to find the optimum condition for membrane preparation.
Polyethersulfone (PES) ultrafiltration (UF) membranes (YMPWSP3001, Sterlitech Corp., USA) with a pore size corresponding to a molecular weight cutoff of 10 kDa were used as the support layers for fabricating the PEM TFC membranes. The PES UF membranes were tested and were found to exhibit a permeation flux of 235.7 L/m2·h at a pressure of 10 bar and temperature of 33.5°C. The molecular structures of the various materials used are shown in Figure 1.
2.2. Fabrication of PEM TFC Membranes
The prepared PEI and PSS solutions were alternately deposited on the PES UF membranes using a spin coater (POLOS SPIN150i®, SPS Inc.). Prior to deposition, the PES UF support membrane was pretreated in an air plasma using a plasma cleaner (PDC-32G-2, Harrick Plasma Inc.) as per a procedure described elsewhere . PEI was deposited firstly on the spinning PES support as the first layer. PSS layer was subsequently deposited in a similar manner to complete one cycle of bilayer deposition. The deposition process was performed at a speed of 3000 rpm; this speed was chosen based on a previous study , as it helped reduce the gradient in the radial thickness from the center of the support . The PEI and PSS solutions were both deposited at a rate of 0.2 mL/s for 10 s, and the film was let to spin-dried for another 20 s afterward. After every polyelectrolyte deposition, the relatively dry film was then rinsed with deionized (DI) water at a rate of 0.4 mL/s for 20 s to remove any weakly bonded polyelectrolyte molecules that might remain on the surface. This was followed by spin-drying for 20 s. The resulting membranes were labelled as (PEI/PSS)x where “x” indicates the number of bilayers. The NaCl concentration in the two polyelectrolyte solutions were the same at 0.05 M optimized value from our previous work [28, 29].
2.3. Permeation Tests
Permeation tests were performed using a crossflow permeation cell (Innovator® CF016, Sterlitech Corporation). The CF016 system has an active membrane surface area of 20.6 cm2. The conditions for the permeation tests were as follows: pressure of 10 bar, feed temperature of 32.39 ± 0.27°C, cross flow velocity (CFV) of 0.65 m/s, and MgCl2 concentration of 6578.21 ± 69.2 ppm. Meanwhile, the pH of the feed solution remained stable at approximately 6.49 ± 0.11 without requiring any adjustments. These tests were performed for 5 h, and the operation conditions were measured every hour.
3. Results and Discussion
PEM membranes consisting of branched PEI/PSS bilayers were fabricated utilizing SA-LbL assembly method on PES UF membrane supports. The resulting membranes were similar to TFC membranes. The multilayer PEI/PSS acted as the active layer for rejecting the salt, while the UF PES support provided the mechanical strength to the overall membrane structure. PSS is a strong polyelectrolyte with a pKa of 2.1 at room temperature , and its degree of ionization remains constant over a wide range of pH values , whereas PEI is weak polyelectrolyte which means the degree of ionization is strongly affected by its pH.
3.1. Effect of Assembly pH on Membrane Performance
As previously mentioned, PEI dissociation in an aqueous solution is a function of pH; meanwhile, the dissociation of polyelectrolyte affects its conformation and multilayer structure. Thus, it is imperative to investigate the effect of assembly pH on membrane performance, i.e., permeate flux and rejection rate. In this work, not only assembly pH of PEI solution was studied, but also that of PSS and the rinse solution were studied too. Previous study by Lutkenhaus et al.  provides a valuable in-depth analysis for the effect of assembly pH of linear PEI (LPEI) on structure of polyelectrolyte multilayer consists of LPEI/PAA.
Figure 2 shows significant improvement of permeability without severely compromising the rejection rate of the membrane when the assembly pH of PEI was kept at 3.5 and that of PSS was changed from 8 to 3.5. This trend is even more pronounced when the water rinse pH was also brought to the same level. This trend implies that external pH also affects the conformation of already deposited PEI.
When the assembly pH of PEI was at 3.5, PEI was in highly ionized state and adopted less coiled conformation; meanwhile, PSS will always have highly flat conformation owing to its fully ionized condition at all pH.
The combination of both polyelectrolytes at the pH for PEI/PSS/water of 3.5/8/7, respectively, is expected to show PEM with higher permeability. However, in fact, it showed the lowest permeability. This observation showed that the external pH also has significant impact. The water and PSS that carry more basic pH will penetrate the already deposited PEI layer and alter PEI ionization state to be less ionized. This results in changing of internal structure and increase of layer thickness. In the end, it provides more barrier for water transport across the film. The opposite behavior was noticed when the pH of rinsing water and PSS were adjusted at the same pH as that of PEI. In this case, PEI chain conformation remains flat and results in higher permeability, whereas when the pH of PEI was adjusted at more basic pH, PEI chain became less ionized and adopted more coiled structure. Therefore, PEM film became thicker and provided less permeability.
Rejection mechanism of the NF membrane is somewhat more complex, particularly for charged solutes as used in this work. It is generally known that there are two contributing mechanisms, i.e., Donnan potential and steric hindrance in the rejection of charged solutes. When the layer was prepared from less ionized PEI, more PEI molecules are needed to compensate the charges of fully ionized PSS. This results in denser film compared to that prepared from highly ionized PEI. The denser film produces higher salt rejection.
3.2. Effect of Number of Bilayers on Membrane Performance
Number of bilayers deposited on membrane is also important parameter which determines the membrane performance. Figure 3 shows the changes in the permeation flux and salt rejection rate as the number of bilayers was increased from 5, 8, 10, and then 20. It shows that as the number of bilayers was increased, the permeate flux decreased. The flux decline can be affected by several things such as layer thickness, effective pore radius, and porosity. However, layer thickness contributes the most significant effect. It is generally known that the permeation flux is inversely proportional to the membrane thickness. Thus, when more layers were added, the layer thickness increased and that resulted in the decrease of the flux. The flux decrease then becomes stagnant as more number of layers were deposited, implying the linear growth of PEI/PSS film as reported somewhere else .
Figure 3 also shows the increase of rejection rate as the number of layers was increased. This trend was due to improvement in surface coverage. This study also suggests that steric hindrance and Donnan potential play an important role in rejection mechanism in the case of NF membrane. Donnan potential effect has already taken place regardless of the number of layers; meanwhile, the steric hindrance effect becomes more evident as the surface coverage and layering quality improved through more layer deposition. This rejection still improved up to a certain number of layers, i.e., around 10 bilayers, and became stagnant afterward. It indicated that at that number of layers, the support has been completely covered.
3.3. Comparison with Other NF Membranes
In this section, the performance of our membrane is compared with other membranes either fabricated using LbL assembly or other techniques as can be seen in Table 1. As shown, membrane produced in this work is comparable to those membranes even when it was tested at 6600 ppm MgCl2, and the membrane still shows stable performance.
In this study, PEM TFC NF membranes consist of PEI/PSS were successfully fabricated using SA-LbL assembly. The fabricated membrane achieved comparable performance with commercial membrane such as NF90 which was tested at the same condition showed rejection rate of 89% and permeate permeability of 4.37 L/h bar·m2. Meanwhile, (PEI/PSS)10–0.05 achieved rejection rate of 93.95% and permeate permeability of 0.9 L/h bar·m2.
In conclusion, the proposed membrane fabrication method is promising, as this method is not limited to a certain type of material. A range of materials, including organic and inorganic materials and even microorganisms have been employed to create thin layers using the conventional dip-LbL assembly technique for various applications. There is still huge room for study and research in this type of membrane including optimization of preparation condition, selection of membrane materials, stability, and so on. Thus, the participation from researchers all over the world is urgently required.
All the data that support the findings of this study are displayed in this manuscript.
Conflicts of Interest
The author declares no conflicts of interest.
This project was funded by the National Plan for Science, Technology, and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, the Kingdome of Saudi Arabia, award #: WAT68-08-R. The author also acknowledges Dr. Farid Fadhillah for his valuable analysis and discussion.
H. Deng, Y. Xu, B. Zhu, X. Wei, F. Liu, and Z. Cui, “Polyelectrolyte membranes prepared by dynamic self-assembly of poly (4-styrenesulfonic acid-co-maleic acid) sodium salt (PSSMA) for nanofiltration (I),” Journal of Membrane Science, vol. 323, no. 1, pp. 125–133, 2008.View at: Publisher Site | Google Scholar
F. Fadhillah, S. M. Javaid Zaidi, Z. Khan, M. Khaled, F. Rahman, and P. Hammond, “Development of multilayer polyelectrolyte thin-film membranes fabricated by spin assisted layer-by-layer assembly,” Journal of Applied Polymer Science, vol. 126, no. 4, pp. 1468–1474, 2012.View at: Publisher Site | Google Scholar
F. Fadhillah, A. M. Alghamdi, M. D. Alsubei, and S. A. Aljlil, “Synthesis of protein-fouling-resistance polyelectrolyte multilayered nanofiltration membranes through spin-assisted layer-by-layer assembly,” Journal of King Saud University—Engineering Sciences, vol. 33, no. 2, pp. 81–87, 2021.View at: Publisher Site | Google Scholar
A. M. Alghamdi and F. Fadhillah, “Thin film composite polyelectrolyte multilayer nanofiltration membrane fabricated using spin assisted layer by layer assembly: application of solution diffusion film model,” Communications in Science and Technology, vol. 5, no. 1, pp. 10–15, 2020.View at: Publisher Site | Google Scholar